Cetirizine hydrochloride
- Product NDC
- 50090-6679
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA209274
- Marketing category
- ANDA
- Substance
- CETIRIZINE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-6679-0 | 30 TABLET, COATED in 1 BOTTLE (50090-6679-0) | 2023-09-11 | No | Historical | |
| 50090-6679-1 | 90 TABLET, COATED in 1 BOTTLE (50090-6679-1) | 2023-09-13 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Cetrizine Hydrochloride Tablets | A-S Medication Solutions | 2023-09-14 | HUMAN OTC DRUG LABEL | 4 |