NDC 11695-6935-2 - Carprofen

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
11695-6935
Requested NDC
11695-6935-2
Package NDCs from labels
11695-6935-1, 11695-6935-2
Manufacturer
BUTLER ANIMAL HEALTH SUPPLY, LLC dba COVETRUS NORTH AMERICA | Norbrook Laboratories Limited
Effective date
2023-09-26
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
covetrus ®BUTLER ANIMAL HEALTH SUPPLY, LLC dba COVETRUS NORTH AMERICA | Norbrook Laboratories Limited2023-09-26PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11695-6935-1Carprofen2 in 1 CARTONINJECTION, SOLUTION23
11695-6935-1Carprofen20 mL in 1 VIAL, GLASSINJECTION, SOLUTION203
11695-6935-2Carprofen50 mL in 1 VIAL, GLASSINJECTION, SOLUTION503
11695-6935-2Carprofen1 in 1 CARTONINJECTION, SOLUTION13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11695-6935CARPROFEN INJECTION, SOLUTION [BUTLER ANIMAL HEALTH SUPPLY, LLC DBA COVETRUS NORTH AMERICA]34 package rows20230928_972f8cfd-ff4d-4e66-9011-b36dc786e9be.zip

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.