Meds A-Z
Insulin
Detailed information about Insulin
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 reduction of hyperglycemia and hyperglycemia-associated clinical signs in dogs with diabetes mellitus.
What it does:
For the reduction of hyperglycemia and hyperglycemia-associated clinical signs in dogs with diabetes mellitus. For the reduction of hyperglycemia and hyperglycemia-associated clinical signs in cats with diabetes mellitus...
When it's needed:
Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Use of a syringe other than a U-40 syringe will...
Call your vet sooner if you notice:
- Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Use of a syringe other than a U-40 syringe will result in incorrect dosing. For subcutaneous injection in cats only.
Commonly reported reactions:
- (2 reports)
- (2 reports)
- (1 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?
Insulin
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/141236 · official_label · FDA application profile
- https://animaldrugsatfda.fda.gov/adafda/views/#/home/previewsearch/141297 · 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. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Use of a syringe other than a U-40 syringe will result in incorrect dosing. For subcutaneous injection in cats only.
- High: Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Use of a syringe other than a U-40 syringe will result in incorrect dosing. For subcutaneous injection in cats only.
- 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 | |
| 1 | Cat | 1 | |
| 1 | Dog | 1 | |
| 1 | Dog | 1 | |
| 1 | Cat | 1 | |
| 1 | Cat | 1 | |
| 1 | Dog | 1 |
Species coverage: Cat (17) Dog (15)
View detailed reaction table
| Reaction | Species | Seriousness | Frequency | Reports |
|---|---|---|---|---|
| Dog | 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 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Non-serious | - | 1 | |
| Dog | Non-serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Non-serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Non-serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 |
- https://api.fda.gov/animalandveterinary/event.json · adverse_reaction · openFDA case USA-USFDACVM-2025-US-047097
Storage & Handling
No storage/handling guidance is linked yet.
Documents
Official label facts are separated from secondary summaries.
Official documents: 12 • Secondary summaries: 0
- UCM391560.pdf · FOI
- UCM374300.pdf · FOI
- ucm118049.pdf · FOI
- ucm118048.pdf · FOI
- CIS VETSULIN N141236C0179-2.pdf · Labeling
- PI VETSULIN N141236C0179.pdf · Labeling
- Vetsulin® · SPL
- FOI Summary sN 141-297 Approved February 8, 2019.pdf · FOI
- UCM198121.pdf · FOI
- Final Version PROZINC N141297.pdf · Labeling
- Final Version PROZINC N141297.pdf · Labeling
- ProZinc® · SPL
No source yet.
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/781 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/780 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/779 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/778 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadLabeling/915 · document · Labeling
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadLabeling/916 · document · Labeling
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/283/Vetsulin%C2%AE · document · SPL
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/6708 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/861 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadLabeling/895 · document · Labeling
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, 11:04 AM UTC
- openFDA case summaries: Source FDA openFDA | Refreshed Feb 9, 2026, 3:22 AM 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. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Use of a syringe other than a U-40 syringe will result in incorrect dosing. For subcutaneous injection in cats only. (Contraindication, High)
Identifiers & Packages
Normalized identifiers (NDC/NADA/ANADA) and package metadata from regulator listings.
| Package NDC | Product NDC | Form / Route | Status |
|---|---|---|---|
| 0010-4499-01 | 0010 | - | |
| 0010-4499-02 | 0010 | - | |
| 57926-490-62 | 57926 | - | |
| 57926-490-69 | 57926 | - |
Enriched Documents
Documents are tiered by source trust: Official, Clinical, Manufacturer, Marketing.
-
PI VETSULIN N141236C0179.pdf
• Official label • Official
• July 1, 2024
FDA official labeling for application 141236
-
CIS VETSULIN N141236C0179-2.pdf
• Official label • Official
• July 1, 2024
FDA official labeling for application 141236
-
ucm118048.pdf
• FOI summary • Official
• July 1, 2024
FDA FOI summary for application 141236
-
ucm118049.pdf
• FOI summary • Official
• July 1, 2024
FDA FOI summary for application 141236
-
UCM374300.pdf
• FOI summary • Official
• July 1, 2024
FDA FOI summary for application 141236
-
UCM391560.pdf
• FOI summary • Official
• July 1, 2024
FDA FOI summary for application 141236
-
Final Version PROZINC N141297.pdf
• Official label • Official
• Nov. 13, 2023
FDA official labeling for application 141297
-
Final Version PROZINC N141297.pdf
• Official label • Official
• Nov. 13, 2023
FDA official labeling for application 141297
-
UCM198121.pdf
• FOI summary • Official
• Nov. 13, 2023
FDA FOI summary for application 141297
-
FOI Summary sN 141-297 Approved February 8, 2019.pdf
• FOI summary • Official
• Nov. 13, 2023
FDA FOI summary for application 141297
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. Federal law restricts this drug to use by or on the order of a licensed v… (Official, 2026-02-12)
- side_effects: Top reported reactions (openFDA): Hyperglycaemia, Vomiting, Lethargy (see also Central nervous system depression in 'Neurological'), Diarrhoea, Weight loss, Hy… (Official, 2026-02-12)
- usage: For the reduction of hyperglycemia and hyperglycemia-associated clinical signs in dogs with diabetes mellitus. For the reduction of hyperglycemia and hyperglyc… (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 |
|---|---|---|---|---|
|
Vetsulin®
RX
Porcine insulin zinc suspension
Liquid (Suspension)
• Subcutaneous
|
Intervet, Inc. | NADA 141-236 | Approved | Jul 1, 2024 |
|
ProZinc®
RX
Insulin
Liquid (Suspension)
• Subcutaneous
|
Boehringer lngelheim Animal Health USA, Inc. | NADA 141-297 | Approved | Nov 13, 2023 |
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 reduction of hyperglycemia and hyperglycemia-associated clinical signs in cats with diabetes mellitus.
Administer an initial dose of 1 to 2 IU by subcutaneous injection. Injections should be given twice daily at approximately 12-hour intervals. For cats fed twice daily, the injections should be concurrent with or right after a meal. For cats fed ad libitum, no change in feeding is needed. Adjust the dose at appropriate intervals based on clinical signs, urinalysis results, and glucose curve values until adequate glycemic control has been attained.
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
For the reduction of hyperglycemia and hyperglycemia-associated clinical signs in dogs with diabetes mellitus.
Starting dose: The recommended starting dose for ProZinc® is 0.2-0.5 IU insulin/pound of body weight (0.5-1.0 IU/kg) once daily. The recommended starting dose for naïve dogs is the lower end of the dose range. The recommended starting dose for dogs with poorly controlled diabetes mellitus and transitioning from another insulin product is the mid to higher end of the dose range based on the veterinarian’s experience with the dog’s medical history and previous insulin dose. When transitioning from another insulin, the dog’s blood glucose and general condition should be closely monitored. When transitioning from another insulin, ProZinc® should be started once daily regardless of the frequency of prior insulin use.
The dose should be given concurrently with or right after a meal. The veterinarian should re-evaluate the dog at appropriate intervals and adjust the dose and frequency based on both clinical signs and laboratory test results (the blood glucose curve values and shape, nadir, and fructosamine) until adequate glycemic control has been attained. In the effectiveness field study, glycemic control was considered adequate if the glucose nadir from a 9-hour blood glucose curve was between 80 and 125 mg/dL, the maximum blood glucose was lessThanEqualTo 300 mg/dL, and clinical signs of hyperglycemia such as polyuria, polydipsia, or weight loss were improved.
Changing to twice daily dosing: Twice daily dosing should be considered if the duration of insulin action is determined to be inadequate with once daily dosing. Use caution when adjusting from once daily to twice daily dosing because ProZinc® may have prolonged duration of action in some dogs. The veterinarian should closely monitor the duration of action using blood glucose curves to avoid the increased risk of hypoglycemia. If twice daily dosing is initiated, the two doses should each be approximately 25% less than the once daily dose required to attain an acceptable glucose nadir. For example, if a dog receiving 10 units of ProZinc® once daily has an acceptable nadir but inadequate duration of activity, the dose should be changed to 7 units twice daily (round down to the nearest whole unit).
Further adjustments in the dosage may be necessary with changes in the dog’s diet, body weight, or concomitant medication, or if the dog develops concurrent infection, inflammation, neoplasia, or an additional endocrine or other medical disorder.
FDA page: Open in Animal Drugs @ FDA
Official Documents (FDA)
Direct links to FDA-hosted PDFs and SPL packages (when available).
-
FOI UCM391560.pdf
Summary
The effect of the supplementis to add a 2.7 mL cartridge presentation for use with the VETPEN automatic injection device. -
FOI UCM374300.pdf
Summary
The effect of the supplement is to change the specification for non-extractable (NE) insulin. -
FOI ucm118049.pdf
Summary
This supplement provides for a new starting dose in dogs and for the use of VETSULIN in cats. -
FOI ucm118048.pdf
Summary
For the reduction of hyperglycemia and hyperglycemia associated clinical signs with diabetes mellitus. -
Labeling CIS VETSULIN N141236C0179-2.pdf
-
Labeling PI VETSULIN N141236C0179.pdf
- Vetsulin® (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
Summary
This supplement provides for the addition of the indication for the reduction of hyperglycemia and hyperglycemia-associated clinical signs in dogs with diabetes mellitus.
-
FOI UCM198121.pdf
Summary
For the reduction of hyperglycemia and hyperglycemia-associated clinical signs in cats with diabetes mellitus. -
Labeling Final Version PROZINC N141297.pdf
-
Labeling Final Version PROZINC N141297.pdf
- ProZinc® (ZIP)
FDA page: Open in Animal Drugs @ FDA
Usage
For the reduction of hyperglycemia and hyperglycemia-associated clinical signs in dogs with diabetes mellitus. For the reduction of hyperglycemia and hyperglycemia-associated clinical signs in cats with diabetes mellitus.
Source: FDA Animal Drugs @ FDA • Reference
Contraindications
Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Use of a syringe other than a U-40 syringe will result in incorrect dosing. For subcutaneous injection in cats only.
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, ['Beagle', 'Terrier (unspecified)'], Female, 11 year, 21.772 kilogram • Drug: MSK, Unassigned, Unknown • Reactions: Head tremor, Hypermetria, Underdose • Outcome: Recovered/Normal
- Report ID: USA-USFDACVM-2025-US-054757
- Serious AE: No
- Treated For AE: No
- Sex: Female
- Age: 11.00 Year
- Weight: 21.772 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
- Form: Unassigned
Cat, Domestic Longhair, Female, 15 year, 4.3 kilogram • Drug: MSK, Unknown • Reactions: Ketosis, Death, Diabetic ketoacidosis, Unresponsive to stimuli • Outcome: Ongoing, Died
- Report ID: USA-USFDACVM-2025-US-052696
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Female
- Age: 15.00 Year
- Weight: 4.300 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
Cat, Domestic Shorthair, Female, 8.5 year, 3.31 kilogram • Drug: MSK, Unknown • Reactions: Vomiting, Hypothermia, Not eating, Elevated alanine aminotransferase, Hypokalaemia… • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-052701
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Female
- Age: 8.50 Year
- Weight: 3.310 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
Cat, Manx, Male • Drug: MSK, Unknown • Reactions: Diarrhea, Digestive tract neoplasm NOS, Death by euthanasia • Outcome: Euthanized
- Report ID: USA-USFDACVM-2025-US-052826
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Male
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
Dog, ['American Pit Bull Terrier', 'Dog (unknown)'], Male, 11.5 year, 29.1 kilogram • Drug: MSK, Subcutaneous • Reactions: Weight loss, Urinary tract infection, High blood pressure, Decreased appetite, Inappropriate urination… • Outcome: Outcome Unknown
- Report ID: USA-USFDACVM-2025-US-052739
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Male
- Age: 11.50 Year
- Weight: 29.100 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Subcutaneous
Cat, Domestic Mediumhair, Female, 11 year, 3.583 kilogram • Drug: MSK, Unknown • Reactions: Vomiting • Outcome: Recovered/Normal
- Report ID: USA-USFDACVM-2025-US-072424
- Serious AE: No
- Treated For AE: No
- Sex: Female
- Age: 11.00 Year
- Weight: 3.583 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
Cat, Domestic Shorthair, Female, 13 year, 4.9 kilogram • Drug: MSK, Unknown • Reactions: Other abnormal test result NOS, Weight loss, Glucosuria, Hyperglycaemia, Ketosis… • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-049767
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Female
- Age: 13.00 Year
- Weight: 4.900 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
Dog, Dog (unknown), Female, 14 year, 17.3 kilogram • Drug: MSK • Reactions: Collapse NOS, Death • Outcome: Died
- Report ID: USA-USFDACVM-2025-US-047097
- Serious AE: Yes
- Treated For AE: No
- Sex: Female
- Age: 14.00 Year
- Weight: 17.300 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
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.
Share Your Thoughts
Let others know your experience or advice regarding this medication.
This medication has not been reviewed by a veterinarian yet.