FDA NDC Directory · JSON-LD · Markdown
NDC 68788-8872 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Generic name | hydroxyzine hydrochloride |
|---|---|
| Labeler / Manufacturer | Preferred Pharmaceuticals Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA217652 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | HYDROXYZINE DIHYDROCHLORIDE (10 mg/1) |
| Marketing started | 20250501 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).