Hydroxyzine Hydrochloride
- Product NDC
- 71610-735
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydroxyzine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA040602
- Marketing category
- ANDA
- Substance
- HYDROXYZINE DIHYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-735-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71610-735-30) | 2023-09-14 | | No | Historical |
| 71610-735-53 | 60 TABLET, FILM COATED in 1 BOTTLE (71610-735-53) | 2023-09-14 | | No | Historical |
| 71610-735-60 | 90 TABLET, FILM COATED in 1 BOTTLE (71610-735-60) | 2023-09-14 | | No | Historical |
| 71610-735-70 | 120 TABLET, FILM COATED in 1 BOTTLE (71610-735-70) | 2023-09-14 | | No | Historical |
| 71610-735-80 | 180 TABLET, FILM COATED in 1 BOTTLE (71610-735-80) | 2023-09-14 | | No | Historical |