FDA NDC Directory · JSON-LD · Markdown
NDC 71205-207 · HUMAN OTC DRUG · TABLET
| Generic name | Cetirizine Hydrochloride |
|---|---|
| Labeler / Manufacturer | Proficient Rx LP |
| Marketing category | Abbreviated NDA (generic) · App ANDA078336 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | CETIRIZINE HYDROCHLORIDE (10 mg/1) |
| Marketing started | 20071227 |
| Package count | 6 |
Source: openFDA. Public-domain (CC0).