Meds A-Z
Meloxicam
Detailed information about Meloxicam
Pet Owner Quick Guide
Start here: what this medicine is for, what it does, and when it's usually needed.
Usually used for:
For the control of pain and inflammation associated with osteoarthritis in dogs.
What it does:
For the control of pain and inflammation associated with osteoarthritis. For the control of postoperative pain and inflammation associated with orthopedic surgery, ovariohysterectomy, and castration when administered pri...
When it's needed:
Federal law restricts this drug to use by or on the order of a licensed veterinarian. For oral use in dogs only. Do not use in cats. Acute renal failure and death have been associated with the use of meloxicam in cats. F...
Call your vet sooner if you notice:
- Federal law restricts this drug to use by or on the order of a licensed veterinarian. For oral use in dogs only. Do not use in cats. Acute renal failure and death have been associated with the use of meloxicam in cats. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Repeated use of meloxicam in cats has been associated with acute renal failure and death. Do not administer additional injectable or oral meloxicam to cats. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Commonly reported reactions:
- (2 reports)
- (2 reports)
- (2 reports)
What to ask your vet today:
- Is this medicine the right fit for my pet’s current symptoms?
- Which warning signs mean I should call back right away?
- How should I handle missed doses or refusal to take the medicine?
Meloxicam
Drug type: Generic ingredient • Branded profile • FDA branded products available
Species: Both
Manufacturer: MSK
Quick Facts
Official label facts first, then secondary summaries. Marketing content is separated below.
- https://animaldrugsatfda.fda.gov/adafda/views/#/home/previewsearch/200794 · official_label · FDA application profile
- https://animaldrugsatfda.fda.gov/adafda/views/#/home/previewsearch/200817 · official_label · FDA application profile
- https://animaldrugsatfda.fda.gov · fda_animal_drugs · Medication usage source
Warnings / Contraindications
Federal law restricts this drug to use by or on the order of a licensed veterinarian. For oral use in dogs only. Do not use in cats. Acute renal failure and death have been associated with the use of meloxicam in cats. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Repeated use of meloxicam in cats has been associated with acute renal failure and death. Do not administer additional injectable or oral meloxicam to cats. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
- High: Federal law restricts this drug to use by or on the order of a licensed veterinarian. For oral use in dogs only. Do not use in cats. Acute renal failure and death have been associated with the use of meloxicam in cats. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Repeated use of meloxicam in cats has been associated with acute renal failure and death. Do not administer additional injectable or oral meloxicam to cats. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
- https://animaldrugsatfda.fda.gov · fda_animal_drugs · Contraindication source
Adverse Reactions
Snapshot first, detailed rows second. This section summarizes signal data and is not a diagnosis.
Tap or hover a reaction to see what it means in plain language.
Most Reported Reactions
| Reaction | Cases | Species | Serious cases |
|---|---|---|---|
| 2 | Cat, Dog | 2 | |
| 2 | Cat, Dog | 2 | |
| 2 | Cat, Dog | 2 | |
| 1 | Cat | 1 | |
| 1 | Cat | 1 | |
| 1 | Dog | 1 | |
| 1 | Cat | 1 | |
| 1 | Cat | 1 |
Species coverage: Cat (21) Dog (11)
View detailed reaction table
| Reaction | Species | Seriousness | Frequency | Reports |
|---|---|---|---|---|
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Non-serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Non-serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Non-serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 |
- https://api.fda.gov/animalandveterinary/event.json · adverse_reaction · openFDA case USA-USFDACVM-2025-US-054641
Storage & Handling
No storage/handling guidance is linked yet.
Documents
Official label facts are separated from secondary summaries.
Official documents: 41 • Secondary summaries: 0
- FOI Summary oA 200-794 Approved August 14, 2025.pdf · FOI
- Meloxisol™ · SPL
- FOI Summary oA 200-817 Approved July 21, 2025.pdf · FOI
- Meloxicam Oral Suspension · SPL
- FOI Summary oA 200-816 Approved July 11, 2025.pdf · FOI
- Meloxisol™ · SPL
- FOI Summary oA 200-727 Approved July 29, 2022.pdf · FOI
- A-200727-G-0031-FL-AA_PI.pdf · Labeling
- Meloxicam · SPL
- ucm118027.pdf · FOI
- ucm118026.pdf · FOI
- N-141219-C-0098-NL-AA_PI.pdf · Labeling
- Metacam® 5 mg/mL Solution for Injection · SPL
- ucm118008.pdf · FOI
- ucm118006.pdf · FOI
- UCM050394.pdf · Labeling
- UCM422143.pdf · Labeling
- N-141213-G-0122-FL-AA_CIS.pdf · Labeling
- N-141213-G-0122-FL-AA_CIS.pdf · Labeling
- Metacam® Oral Suspension · SPL
- UCM338146.pdf · FOI
- A-200485-C-0047-NL-AA_PI.pdf · Labeling
- Meloxicam Injection · SPL
- UCM338160.pdf · FOI
- A-200491-C-0034-NL-AA_PI.pdf · Labeling
- Loxicom® · SPL
- UCM417720.pdf · FOI
- A-200540-C-0029-NL-AA_PI.pdf · Labeling
- Meloxicam Solution for Injection · SPL
- UCM449223.pdf · FOI
- A200497_Client_Info_Sheet.pdf · Labeling
- A200497_Package_Insert.pdf · Labeling
- Loxicom® · SPL
- UCM370746.pdf · FOI
- ANADA 200550 Package Insert and Client Info Sheet for Dogs.pdf · Labeling
- ANADA 200550 Package Insert and Client Info Sheet for Dogs.pdf · Labeling
- Meloxidyl® · SPL
- UCM338139.pdf · FOI
- UCM342580.pdf · Labeling
- UCM422174.pdf · Labeling
- OroCAM® Transmucosal Oral Spray · SPL
No source yet.
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/17325 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/17646/Meloxisol%E2%84%A2 · document · SPL
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/17255 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/17566/Meloxicam%20Oral%20Suspension · document · SPL
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/17209 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/17527/Meloxisol%E2%84%A2 · document · SPL
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/12709 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadLabeling/2019 · document · Labeling
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/12806/Meloxicam · document · SPL
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/751 · document · FOI
Promotional Materials (Marketing)
This content is marketing material and not clinical guidance.
No marketing assets are linked yet.
No source yet.
Technical appendix (vet reference)
Canonical medication sections are above. This legacy block remains available for deeper cross-reference without cluttering the primary workflow.
At a Glance
Quick facts and links to official labeling and safety signals.
- Medication catalog: Source PetWisePlus | Refreshed Feb 12, 2026, 10:44 PM UTC
-
Animal Drugs @ FDA:
Source FDA
| Refreshed Feb 16, 2026, 11:00 AM UTC
Applications/products are imported from FDA export data.
-
Animal Drugs @ FDA previews:
Source FDA
| Refreshed Feb 9, 2026, 3:05 AM UTC
Label highlights/doc links are fetched from FDA preview endpoints.
-
Animal Drug Product Listing Directory (NDC):
Source FDA
| Refreshed Feb 16, 2026, 11:00 AM UTC
Package/product NDCs from FDA’s electronic listing directory (XLS).
- openFDA reaction terms: Source FDA openFDA | Refreshed Feb 16, 2026, 11:02 AM UTC
- openFDA case summaries: Source FDA openFDA | Refreshed Feb 12, 2026, 10:42 PM UTC
Counseling and Monitoring Highlights
Global Pet owner/Vet mode is controlled in the header. This section avoids duplicate in-page persona tabs.
- Federal law restricts this drug to use by or on the order of a licensed veterinarian. For oral use in dogs only. Do not use in cats. Acute renal failure and death have been associated with the use of meloxicam in cats. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Repeated use of meloxicam in cats has been associated with acute renal failure and death. Do not administer additional injectable or oral meloxicam to cats. Federal law restricts this drug to use by or on the order of a licensed veterinarian. (Contraindication, High)
Identifiers & Packages
Normalized identifiers (NDC/NADA/ANADA) and package metadata from regulator listings.
| Package NDC | Product NDC | Form / Route | Status |
|---|---|---|---|
| 0010-6013-01 | 0010 | - | |
| 0010-6014-01 | 0010 | - | |
| 0010-6014-02 | 0010 | - | |
| 0010-6015-01 | 0010 | - | |
| 0010-6015-02 | 0010 | - | |
| 0010-6015-03 | 0010 | - | |
| 0010-6015-04 | 0010 | - | |
| 11695-6936-1 | 11695 | - | |
| 11695-6936-2 | 11695 | - | |
| 11695-6966-1 | 11695 | - | |
| 11695-6966-2 | 11695 | - | |
| 11695-6966-3 | 11695 | - | |
| 11695-6966-4 | 11695 | - | |
| 11695-7008-1 | 11695 | - | |
| 11695-7008-2 | 11695 | - | |
| 13744-505-01 | 13744 | - | |
| 13744-505-10 | 13744 | - | |
| 13744-505-20 | 13744 | - | |
| 13744-505-32 | 13744 | - | |
| 13985-559-10 | 13985 | - |
Enriched Documents
Documents are tiered by source trust: Official, Clinical, Manufacturer, Marketing.
-
FOI Summary oA 200-794 Approved August 14, 2025.pdf
• FOI summary • Official
• Aug. 28, 2025
FDA FOI summary for application 200794
-
FOI Summary oA 200-817 Approved July 21, 2025.pdf
• FOI summary • Official
• July 31, 2025
FDA FOI summary for application 200817
-
FOI Summary oA 200-816 Approved July 11, 2025.pdf
• FOI summary • Official
• July 31, 2025
FDA FOI summary for application 200816
-
A-200727-G-0031-FL-AA_PI.pdf
• Official label • Official
• Nov. 7, 2024
FDA official labeling for application 200727
-
FOI Summary oA 200-727 Approved July 29, 2022.pdf
• FOI summary • Official
• Nov. 7, 2024
FDA FOI summary for application 200727
-
N-141219-C-0098-NL-AA_PI.pdf
• Official label • Official
• March 1, 2024
FDA official labeling for application 141219
-
ucm118026.pdf
• FOI summary • Official
• March 1, 2024
FDA FOI summary for application 141219
-
ucm118027.pdf
• FOI summary • Official
• March 1, 2024
FDA FOI summary for application 141219
-
N-141213-G-0122-FL-AA_CIS.pdf
• Official label • Official
• Dec. 21, 2023
FDA official labeling for application 141213
-
N-141213-G-0122-FL-AA_CIS.pdf
• Official label • Official
• Dec. 21, 2023
FDA official labeling for application 141213
-
UCM422143.pdf
• Official label • Official
• Dec. 21, 2023
FDA official labeling for application 141213
-
UCM050394.pdf
• Official label • Official
• Dec. 21, 2023
FDA official labeling for application 141213
-
ucm118006.pdf
• FOI summary • Official
• Dec. 21, 2023
FDA FOI summary for application 141213
-
ucm118008.pdf
• FOI summary • Official
• Dec. 21, 2023
FDA FOI summary for application 141213
-
A-200485-C-0047-NL-AA_PI.pdf
• Official label • Official
• Jan. 31, 2023
FDA official labeling for application 200485
-
UCM338146.pdf
• FOI summary • Official
• Jan. 31, 2023
FDA FOI summary for application 200485
-
A-200491-C-0034-NL-AA_PI.pdf
• Official label • Official
• Aug. 2, 2021
FDA official labeling for application 200491
-
UCM338160.pdf
• FOI summary • Official
• Aug. 2, 2021
FDA FOI summary for application 200491
-
A-200540-C-0029-NL-AA_PI.pdf
• Official label • Official
• Aug. 18, 2020
FDA official labeling for application 200540
-
UCM417720.pdf
• FOI summary • Official
• Aug. 18, 2020
FDA FOI summary for application 200540
-
A200497_Package_Insert.pdf
• Official label • Official
• Feb. 27, 2019
FDA official labeling for application 200497
-
A200497_Client_Info_Sheet.pdf
• Official label • Official
• Feb. 27, 2019
FDA official labeling for application 200497
-
UCM449223.pdf
• FOI summary • Official
• Feb. 27, 2019
FDA FOI summary for application 200497
-
ANADA 200550 Package Insert and Client Info Sheet for Dogs.pdf
• Official label • Official
• Dec. 21, 2018
FDA official labeling for application 200550
-
ANADA 200550 Package Insert and Client Info Sheet for Dogs.pdf
• Official label • Official
• Dec. 21, 2018
FDA official labeling for application 200550
-
UCM370746.pdf
• FOI summary • Official
• Dec. 21, 2018
FDA FOI summary for application 200550
-
UCM422174.pdf
• Official label • Official
• Nov. 13, 2017
FDA official labeling for application 141346
-
UCM342580.pdf
• Official label • Official
• Nov. 13, 2017
FDA official labeling for application 141346
-
UCM338139.pdf
• FOI summary • Official
• Nov. 13, 2017
FDA FOI summary for application 141346
Data Sources & Revision History
Every non-trivial field is expected to include provenance and update timestamps.
- contraindications: Federal law restricts this drug to use by or on the order of a licensed veterinarian. For oral use in dogs only. Do not use in cats. Acute renal failure and de… (Official, 2026-02-12)
- side_effects: Top reported reactions (openFDA): Vomiting, Diarrhoea, Lethargy (see also Central nervous system depression in 'Neurological'), Anorexia, Death by euthanasia, … (Official, 2026-02-12)
- usage: For the control of pain and inflammation associated with osteoarthritis. For the control of postoperative pain and inflammation associated with orthopedic surg… (Official, 2026-02-12)
- side_effects updated 2026-02-12 22:44 by etl_backfill • Backfilled from existing medication fields
- contraindications updated 2026-02-12 22:44 by etl_backfill • Backfilled from existing medication fields
- usage updated 2026-02-12 22:44 by etl_backfill • Backfilled from existing medication fields
FDA Products & Applications (Animal Drugs @ FDA)
Official sponsor/proprietary-name/application-status records linked by active ingredient.
| Product | Sponsor | Application | Status | Published |
|---|---|---|---|---|
|
Meloxisol™
RX
Meloxicam
Oral Suspension
• Oral
|
Cronus Pharma Specialities India Private Ltd. | ANADA 200-794 | Approved | Aug 28, 2025 |
|
Meloxicam Oral Suspension
RX
Meloxicam
Oral Suspension
• Oral
|
Felix Pharmaceuticals Pvt. Ltd. | ANADA 200-817 | Approved | Jul 31, 2025 |
|
Meloxisol™
RX
Meloxicam
Oral Suspension
• Oral
|
Cronus Pharma Specialities India Private Ltd. | ANADA 200-816 | Approved | Jul 31, 2025 |
|
Meloxicam
RX
Meloxicam
Injectable Solution
• Intravenous, Subcutaneous
|
Felix Pharmaceuticals Pvt. Ltd. | ANADA 200-727 | Approved | Nov 7, 2024 |
|
Metacam® 5 mg/mL Solution for Injection
RX
Meloxicam
Liquid (Solution)
• Subcutaneous, Intravenous
|
Boehringer lngelheim Animal Health USA, Inc. | NADA 141-219 | Approved | Mar 1, 2024 |
|
Metacam® Oral Suspension
RX
Meloxicam
Liquid (Suspension)
• Oral
|
Boehringer lngelheim Animal Health USA, Inc. | NADA 141-213 | Approved | Dec 21, 2023 |
|
Meloxicam Injection
RX
Meloxicam
Sterile Solution
• Subcutaneous, Intravenous
|
Accord Healthcare, Inc. | ANADA 200-485 | Approved | Jan 31, 2023 |
|
Loxicom®
RX
Meloxicam
Solution For Injection
• Intravenous, Subcutaneous
|
Norbrook Laboratories, Ltd. | ANADA 200-491 | Approved | Aug 2, 2021 |
|
Meloxicam Solution for Injection
RX
Meloxicam
Sterile Solution
• Intravenous, Subcutaneous
|
Dechra Veterinary Products LLC | ANADA 200-540 | Approved | Aug 18, 2020 |
|
Loxicom®
RX
Meloxicam
Oral Suspension
• Oral
|
Norbrook Laboratories, Ltd. | ANADA 200-497 | Approved | Feb 27, 2019 |
|
Meloxidyl®
RX
Meloxicam
Oral Suspension
• Oral
|
Ceva Sante Animale | ANADA 200-550 | Approved | Dec 21, 2018 |
|
OroCAM® Transmucosal Oral Spray
RX
Meloxicam
Transmucosal Oral Spray
• Oral
|
Zoetis Inc. | NADA 141-346 | Approved | Nov 13, 2017 |
Data source: FDA Animal Drugs @ FDA (public search export).
What It's For (FDA Label Highlights)
Extracted from FDA Animal Drugs @ FDA product labeling. Always confirm details with your veterinarian.
Composition / specifications
For the control of pain and inflammation associated with osteoarthritis in dogs.
Administer orally as a single dose at 0.09 mg per pound (mg/lb) body weight (0.2 mg per kilogram (mg/kg)) on the first day of treatment. For all treatments after day 1, administer 0.045 mg/lb (0.1 mg/kg) body weight once daily.
FDA page: Open in Animal Drugs @ FDA
For the control of pain and inflammation associated with osteoarthritis.
Administer orally as a single dose at 0.09 mg per pound (mg/lb) body weight (0.2 mg per kilogram (mg/kg)) on the first day of treatment. For all treatments after day 1, administer 0.045 mg/lb (0.1 mg/kg) body weight once daily.
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
For the control of pain and inflammation associated with osteoarthritis in dogs.
Administer orally as a single dose at 0.09 mg per pound (mg/lb) body weight (0.2 mg per kilogram (mg/kg)) on the first day of treatment. For all treatments after day 1, administer 0.045 mg/lb (0.1 mg/kg) body weight once daily.
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
For the control of pain and inflammation associated with osteoarthritis.
Meloxicam injection should be administered initially as a single dose, at0.09 mg/lb (0.2 mg/kg) body weight intravenously (IV) or subcutaneously (SQ), followed, after 24 hours, by meloxicam oral suspension at the daily dose of 0.045mg/lb (0.1 mg/kg) body weight, either mixed with food or placed directly in the mouth.
For the control of postoperative pain and inflammation associated with orthopedic surgery, ovariohysterectomy and castration when administered prior to surgery.
Administer a single, one-time subcutaneous dose of Meloxicam injection to cats at a dose of 0.14 mg/lb (0.3 mg/kg) body weight. Use of additional meloxicam or other NSAIDs is contraindicated. To ensure accuracy of dosing, the use of a 1 mL graduated syringe is recommended.
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
Administer initially as a single dose at 0.09 mg/lb (0.2 mg/kg) body weight intravenously (IV) or subcutaneously (SQ), followed, after 24 hours, by meloxicam oral suspension at the daily dose of 0.045 mg/lb (0.1 mg/kg) body weight, either mixed with food or placed directly in the mouth.
For the control of postoperative pain and inflammation associated with orthopedic surgery, ovariohysterectomy and castration when administered prior to surgery.
Administer a single, one-time subcutaneous dose of 0.14 mg/lb (0.3 mg/kg) body weight. Use of additional meloxicam or other NSAIDs is contraindicated.
Repeated use of meloxicam in cats has been associated with acute renal failure and death. Do not administer additional injectable or oral meloxicam to cats.
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
FDA page: Open in Animal Drugs @ FDA
Official Documents (FDA)
Direct links to FDA-hosted PDFs and SPL packages (when available).
-
Summary
For the control of pain and inflammation associated with osteoarthritis in dogs.
- Meloxisol™ (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
Summary
For the control of pain and inflammation associated with osteoarthritis in dogs.
FDA page: Open in Animal Drugs @ FDA
-
Summary
For the control of pain and inflammation associated with osteoarthritis in dogs.
- Meloxisol™ (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
Summary
Dogs: Meloxicam Injection is indicated in dogs for the control of pain and inflammation associated with osteoarthritis.
Cats: For the control of postoperative pain and inflammation associated with orthopedic surgery, ovariohysterectomy and castration when administered prior to surgery.
-
Labeling A-200727-G-0031-FL-AA_PI.pdf
- Meloxicam (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
FOI ucm118027.pdf
Summary
To add a claim for the control of postoperative pain and inflammation associated with orthopedic surgery, ovariohysterectomy and castration when administered prior to surgery in cats. -
FOI ucm118026.pdf
Summary
METACAM (meloxicam) 5 mg/mL Solution for Injection is indicated for the control of pain and inflammation associated with osteoarthritis in dogs. -
Labeling N-141219-C-0098-NL-AA_PI.pdf
FDA page: Open in Animal Drugs @ FDA
-
FOI ucm118008.pdf
Summary
This supplement to NADA 141-213 provides revisions to 21 CFR 520.1350 (1) Amount. To change the format to read “administered initially at 0.09 mg/lb (0.2 mg/kg) body weight only on the first day of treatment. For all treatments after day 1, METACAM Oral Suspension should be administered once daily at a dose of 0.045 mg/lb (0.1 mg/kg).” -
FOI ucm118006.pdf
Summary
Metacam® Oral Suspension is indicated for the control of pain and inflammation associated with osteoarthritis in dogs. -
Labeling UCM050394.pdf
-
Labeling UCM422143.pdf
-
Labeling N-141213-G-0122-FL-AA_CIS.pdf
-
Labeling N-141213-G-0122-FL-AA_CIS.pdf
- Metacam® Oral Suspension (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
FOI UCM338146.pdf
Summary
Dogs: Meloxicam Injection 5 mg/mL Solution for Injection is indicated for the control of pain and inflammation associated with osteoarthritis.
Cats: For the control of postoperative pain and inflammation associated with orthopedic surgery, ovariohysterectomy and castration when administered prior to surgery. -
Labeling A-200485-C-0047-NL-AA_PI.pdf
- Meloxicam Injection (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
FOI UCM338160.pdf
Summary
Loxicom® (meloxicam) 5 mg/mL Injectable sterile solution is indicated for the control of pain and inflammation associated with osteoarthritis in dogs and for the control of postoperative pain and inflammation associated with orthopedic surgery, ovariohysterectomy and castration when administered prior to surgery in cats. -
Labeling A-200491-C-0034-NL-AA_PI.pdf
- Loxicom® (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
FOI UCM417720.pdf
Summary
Dogs: For the control of pain and inflammation associated with osteoarthritis.
Cats: For the control of postoperative pain and inflammation associated with orthopedic surgery, ovariohysterectomy and castration when administered prior to surgery. -
Labeling A-200540-C-0029-NL-AA_PI.pdf
FDA page: Open in Animal Drugs @ FDA
-
FOI UCM449223.pdf
Summary
For the control of pain and inflammation associated with osteoarthritis in dogs. -
Labeling A200497_Client_Info_Sheet.pdf
-
Labeling A200497_Package_Insert.pdf
- Loxicom® (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
FOI UCM370746.pdf
Summary
For control of pain and inflammation associated with osteoarthritis in dogs.
- Meloxidyl® (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
FOI UCM338139.pdf
Summary
For the control of pain and inflammation associated with osteoarthritis in dogs. -
Labeling UCM342580.pdf
-
Labeling UCM422174.pdf
FDA page: Open in Animal Drugs @ FDA
Usage
For the control of pain and inflammation associated with osteoarthritis. For the control of postoperative pain and inflammation associated with orthopedic surgery, ovariohysterectomy, and castration when administered prior to surgery. For the control of pain and inflammation associated with osteoarthritis in dogs.
Source: FDA Animal Drugs @ FDA • Reference
Contraindications
Federal law restricts this drug to use by or on the order of a licensed veterinarian. For oral use in dogs only. Do not use in cats. Acute renal failure and death have been associated with the use of meloxicam in cats. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Repeated use of meloxicam in cats has been associated with acute renal failure and death. Do not administer additional injectable or oral meloxicam to cats. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Side Effects
No approved side-effect narrative is linked yet.
openFDA reaction signals are available for Dog 56 and Cat 56 (view top reported reactions).
Top Reported Reactions (openFDA)
Aggregated reaction terms from FDA openFDA reports (not verified; does not prove causation).
Data source: FDA openFDA Animal & Veterinary adverse event reports.
Adverse Event Case Summaries (openFDA)
These are individual FDA adverse event reports. They are unverified and do not prove the medication caused the reaction.
Dog, Boxer (German Boxer), Female, 7 year, 29.484 kilogram • Drug: MSK, Suspension, Oral, Dose: 2.93 Milligram per dose, Frequency: 24 per hour • Reactions: Pacing, Loss of appetite, Abdominal pain, Peritoneal fluid, abnormal NOS, Abnormal radiograph finding… • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-054641
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Female
- Age: 7.00 Year
- Weight: 29.484 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Form: Suspension
- Dose: 2.93 Milligram per dose
- Frequency: 24 per hour
Cat, Cat (unknown), Female, 4.05 kilogram • Drug: MSK, Solution, Unknown, Dose: 0.16 Milligram per kilogram • Reactions: Hyperglycaemia • Outcome: Outcome Unknown
- Report ID: USA-USFDACVM-2025-US-054116
- Serious AE: No
- Treated For AE: No
- Sex: Female
- Weight: 4.050 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
- Form: Solution
- Dose: 0.16 Milligram per kilogram
Dog, Terrier - Yorkshire, Female, 5 month, 1.814 kilogram • Drug: MSK, Suspension, Oral, Dose: 0.15 Milligram per kilogram • Reactions: Lack of efficacy (virus) - parvovirus, Death, Diarrhea, Not eating, Not drinking • Outcome: Died
- Report ID: USA-USFDACVM-2025-US-056162
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Female
- Age: 5.00 Month
- Weight: 1.814 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Form: Suspension
- Dose: 0.15 Milligram per kilogram
Dog, Terrier - Yorkshire, Female, 5 month, 1.814 kilogram • Drug: MSK, Injection, Subcutaneous, Dose: 0.06 mL per animal • Reactions: Death • Outcome: Died
- Report ID: USA-USFDACVM-2025-US-056175
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Female
- Age: 5.00 Month
- Weight: 1.814 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Subcutaneous
- Form: Injection
- Dose: 0.06 mL per animal
Cat, Mixed (Cat), Mixed, 11 year • Drug: MSK, Oral, Dose: 0.05 Milligram per kilogram • Reactions: Ulceration NOS, Inappropriate defecation, Crust, Desquamation, Erythema… • Outcome: Recovered/Normal, Died, Outcome Unknown
- Report ID: AUS-USFDACVM-2025-AU-000005
- Serious AE: Yes
- Treated For AE: No
- Sex: Mixed
- Age: 11.00 Year
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Dose: 0.05 Milligram per kilogram
Dog, Retriever - Labrador, Male, 6 year, 48.444 kilogram • Drug: MSK, Unassigned, Oral • Reactions: Hypersensitivity reaction, Localised rash, Overdose, Intentional misuse • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-055182
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Male
- Age: 6.00 Year
- Weight: 48.444 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Form: Unassigned
Dog, Pug, Female, 6 year, 7.8 kilogram • Drug: MSK, Oral, Dose: 0.52 mL per animal, Frequency: 1 per day • Reactions: Diarrhea, Vomiting, Haematochezia • Outcome: Recovered/Normal
- Report ID: GBR-USFDACVM-2025-GB-000062
- Serious AE: No
- Treated For AE: No
- Sex: Female
- Age: 6.00 Year
- Weight: 7.800 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Dose: 0.52 mL per animal
- Frequency: 1 per day
Cat, Domestic Shorthair, Female, 6 year, 4.799 kilogram • Drug: MSK, Suspension, Oral, Dose: 0.09 Milligram per kilogram, Frequency: 1 per day • Reactions: Tiredness (lethargy), Renal failure, Elevated renal parameters, Decreased appetite, Vomiting foam • Outcome: Outcome Unknown
- Report ID: USA-USFDACVM-2025-US-055427
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Female
- Age: 6.00 Year
- Weight: 4.799 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Form: Suspension
- Dose: 0.09 Milligram per kilogram
- Frequency: 1 per day
Data source: FDA openFDA Animal & Veterinary adverse event reports.
Overdose Information
No approved overdose-management text is linked yet. If overdose is suspected, contact a veterinarian or emergency clinic immediately.
Storage & Handling
No approved storage guidance is linked yet for this ingredient. Use manufacturer packaging and veterinary guidance for handling/storage.
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This medication has not been reviewed by a veterinarian yet.