Hydroxyzine hydrochloride
- Product NDC
- 0904-7379
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA204279
- Marketing category
- ANDA
- Substance
- HYDROXYZINE DIHYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 0904-7379-40 | 500 TABLET in 1 BOTTLE (0904-7379-40) | 2023-08-01 | | No | Historical |
| 0904-7379-80 | 1000 TABLET in 1 BOTTLE (0904-7379-80) | 2023-08-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Rx only | Major Pharmaceuticals | 2025-11-10 | HUMAN PRESCRIPTION DRUG LABEL | 4 |