Cetirizine Hydrochloride (Allergy)
- Product NDC
- 50090-6170
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090760
- Marketing category
- ANDA
- Substance
- CETIRIZINE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-6170-0 | 48 BOTTLE in 1 CASE (50090-6170-0) / 30 TABLET in 1 BOTTLE | 2022-10-13 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| 42c9636f-07af-44a3-8d84-c11e1b57783a | A-S Medication Solutions | 2024-07-02 | Human OTC Drug Label | 15 |