FDA NDC Directory · JSON-LD · Markdown
NDC 0781-2145 · HUMAN PRESCRIPTION DRUG · CAPSULE
| Labeler / Manufacturer | Sandoz Inc |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA064082 |
| Dosage form / route | CAPSULE · ORAL |
| Active ingredients | AMPICILLIN TRIHYDRATE (500 mg/1) |
| Marketing started | 19950829 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).