FDA NDC Directory · JSON-LD · Markdown
NDC 0245-0147 · HUMAN PRESCRIPTION DRUG · TABLET
| Generic name | Amiodarone Hydrochloride |
|---|---|
| Labeler / Manufacturer | Upsher-Smith Laboratories, LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA075135 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | AMIODARONE HYDROCHLORIDE (200 mg/1) |
| Marketing started | 20101115 |
| Package count | 4 |
Source: openFDA. Public-domain (CC0).