FDA NDC Directory · JSON-LD · Markdown
NDC 56062-847 · HUMAN OTC DRUG · TABLET, FILM COATED
| Generic name | fexofenadine hydrochloride |
|---|---|
| Labeler / Manufacturer | Publix Super Markets Inc |
| Marketing category | Abbreviated NDA (generic) · App ANDA212971 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | FEXOFENADINE HYDROCHLORIDE (180 mg/1) |
| Marketing started | 20220114 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).