FDA NDC Directory · JSON-LD · Markdown
NDC 51672-2108 · HUMAN OTC DRUG · SOLUTION
| Generic name | Loratadine |
|---|---|
| Labeler / Manufacturer | Taro Pharmaceuticals U.S.A., Inc. |
| Marketing category | Abbreviated NDA (generic) · App ANDA201865 |
| Dosage form / route | SOLUTION · ORAL |
| Active ingredients | LORATADINE (5 mg/5mL) |
| Marketing started | 20161208 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).