FDA NDC Directory · JSON-LD · Markdown
NDC 67751-033 · HUMAN OTC DRUG · TABLET, FILM COATED
| Generic name | FEXOFENADINE HYDROCHLORIDE |
|---|---|
| Labeler / Manufacturer | Navajo Manufacturing Company Inc. |
| Marketing category | New Drug Application (innovator) · App NDA020872 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | FEXOFENADINE HYDROCHLORIDE (180 mg/1) |
| Marketing started | 20150512 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).