FDA NDC Directory · JSON-LD · Markdown
NDC 0781-6157 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION
| Labeler / Manufacturer | Sandoz Inc |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA065378 |
| Dosage form / route | POWDER, FOR SUSPENSION · ORAL |
| Active ingredients | AMOXICILLIN (400 mg/5mL) |
| Marketing started | 20070326 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).