Cetirizine Hydrochloride
- Product NDC
- 51672-2106
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Taro Pharmaceuticals U.S.A., Inc.
- Application
- ANDA201546
- Marketing category
- ANDA
- Substance
- CETIRIZINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 51672-2106-1 | 1 BOTTLE in 1 CARTON (51672-2106-1) / 240 mL in 1 BOTTLE | 2011-05-20 | | No | Historical |
| 51672-2106-4 | 1 BOTTLE in 1 CARTON (51672-2106-4) / 60 mL in 1 BOTTLE | 2011-05-20 | | No | Historical |
| 51672-2106-8 | 1 BOTTLE in 1 CARTON (51672-2106-8) / 120 mL in 1 BOTTLE | 2011-05-20 | | No | Historical |