HYDROXYZINE HYDROCHLORIDE
- Product NDC
- 50090-7329
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxyzine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA217652
- Marketing category
- ANDA
- Substance
- HYDROXYZINE DIHYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-7329-0 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7329-0) | 2024-10-15 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Hydroxyzine Hydrochloride Tablets, USP Rx only | A-S Medication Solutions | 2025-12-02 | HUMAN PRESCRIPTION DRUG LABEL | 1 |