Cetirizine Hydrochloride
- Product NDC
- 50090-5220
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076601
- Marketing category
- ANDA
- Substance
- CETIRIZINE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-5220-0 | 1 BOTTLE in 1 CARTON (50090-5220-0) / 120 mL in 1 BOTTLE | 2020-10-07 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Cetirizine Hydrochloride Oral Solution USP, 5 mg/5 mL (1 mg/mL) | A-S Medication Solutions | 2024-03-14 | HUMAN PRESCRIPTION DRUG LABEL | 6 |