FDA NDC Directory · JSON-LD · Markdown
NDC 72559-028 · HUMAN OTC DRUG · TABLET
| Generic name | Fexofenadine Hydrochloride 180 mg |
|---|---|
| Labeler / Manufacturer | Little Pharma, Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA204507 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | FEXOFENADINE HYDROCHLORIDE (180 mg/1) |
| Marketing started | 20230907 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).