NDC 55529-133-22 - Carprieve
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
- 55529-133
- Requested NDC
- 55529-133-22
- Package NDCs from labels
- 55529-133-20, 55529-133-21, 55529-133-22
- Manufacturer
- Norbrook Laboratories Limited
- Effective date
- 2026-04-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Carprieve - Norbrook Laboratories Limited | Norbrook Laboratories Limited | 2026-04-13 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55529-133-20 | Carprieve | 30 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 30 | 3 | |
| 55529-133-21 | Carprieve | 60 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 60 | 3 | |
| 55529-133-22 | Carprieve | 180 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 180 | 3 |
DailyMed Dashboard NDC Coverage#
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.