Cetirizine Hydrochloride
- Product NDC
- 51655-801
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride Tablets
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA078343
- Marketing category
- ANDA
- Substance
- CETIRIZINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 51655-801-52 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-801-52) | 2023-01-25 | | No | Historical |
| 51655-801-60 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-801-60) | 2023-01-25 | | No | Historical |
| 51655-801-84 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-801-84) | 2023-01-25 | | No | Historical |