Cetirizine Hydrochloride Tablets, 10 mg
- Product NDC
- 25000-220
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- MARKSANS PHARMA LIMITED
- Application
- ANDA078933
- Marketing category
- ANDA
- Substance
- CETIRIZINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 25000-220-03 | 1 BOTTLE in 1 CARTON (25000-220-03) / 30 TABLET in 1 BOTTLE | 2022-01-13 | | No | Historical |
| 25000-220-08 | 1 BOTTLE in 1 CARTON (25000-220-08) / 100 TABLET in 1 BOTTLE | 2022-01-13 | | No | Historical |
| 25000-220-14 | 1000 TABLET in 1 BOTTLE (25000-220-14) | 2022-01-13 | | No | Historical |
| 25000-220-78 | 1 BLISTER PACK in 1 CARTON (25000-220-78) / 7 TABLET in 1 BLISTER PACK | 2023-04-17 | | No | Historical |
| 25000-220-81 | 1 BLISTER PACK in 1 CARTON (25000-220-81) / 14 TABLET in 1 BLISTER PACK | 2023-07-21 | | No | Historical |