Hydroxyzine hydrochloride
- Product NDC
- 71610-844
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA204279
- Marketing category
- ANDA
- Substance
- HYDROXYZINE DIHYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-844-53 | 60 TABLET in 1 BOTTLE (71610-844-53) | 2024-06-28 | | No | Historical |
| 71610-844-60 | 90 TABLET in 1 BOTTLE (71610-844-60) | 2024-06-28 | | No | Historical |
| 71610-844-80 | 180 TABLET in 1 BOTTLE (71610-844-80) | 2024-06-28 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Rx only | Aphena Pharma Solutions - Tennessee, LLC | 2024-06-28 | HUMAN PRESCRIPTION DRUG LABEL | 1 |