FDA NDC Directory · JSON-LD · Markdown
NDC 70518-4408 · HUMAN PRESCRIPTION DRUG · TABLET
| Labeler / Manufacturer | REMEDYREPACK INC. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA076056 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | PRAVASTATIN SODIUM (20 mg/1) |
| Marketing started | 20250728 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).