NDC 26637-513-18 - 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
- 26637-513
- Requested NDC
- 26637-513-18
- Package NDCs from labels
- 26637-513-60, 26637-513-18
- Manufacturer
- Putney, Inc.
- Effective date
- 2017-03-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Carprofen - Putney, Inc. | Putney, Inc. | 2017-03-21 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CARPROFEN | ACTIVE INGREDIENT | FFL0D546HO | CARPROFEN TABLET, CHEWABLE [PUTNEY, INC.] | 1 | |
| CARPROFEN | ACTIVE MOIETY | FFL0D546HO | CARPROFEN TABLET, CHEWABLE [PUTNEY, INC.] | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.