FDA NDC Directory · JSON-LD · Markdown
NDC 41520-229 · HUMAN OTC DRUG · TABLET, FILM COATED
| Generic name | fexofenadine hcl |
|---|---|
| Labeler / Manufacturer | American Sales Company |
| Marketing category | Abbreviated NDA (generic) · App ANDA076447 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | FEXOFENADINE HYDROCHLORIDE (180 mg/1) |
| Marketing started | 20161014 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).