NDC 0010-9160-02 - PREVICOX
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
- 0010-9160
- Requested NDC
- 0010-9160-02
- Package NDCs from labels
- 0010-9160-01, 0010-9160-02, 0010-9160-03
- Manufacturer
- Boehringer Ingelheim Animal Health USA Inc
- Effective date
- 2026-05-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PREVICOX - Boehringer Ingelheim Animal Health USA Inc | Boehringer Ingelheim Animal Health USA Inc | 2026-05-28 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0010-9160-01 | PREVICOX | 3 in 1 CARTON | TABLET, CHEWABLE | 3 | 1 | |
| 0010-9160-01 | PREVICOX | 10 in 1 BLISTER PACK | TABLET, CHEWABLE | 10 | 1 | |
| 0010-9160-02 | PREVICOX | 60 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 60 | 1 | |
| 0010-9160-02 | PREVICOX | 1 in 1 CARTON | TABLET, CHEWABLE | 1 | 1 | |
| 0010-9160-03 | PREVICOX | 180 in 1 BOTTLE, PLASTIC | TABLET, CHEWABLE | 180 | 1 | |
| 0010-9160-03 | PREVICOX | 1 in 1 CARTON | TABLET, CHEWABLE | 1 | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.