FDA NDC Directory · JSON-LD · Markdown
NDC 0093-7446 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE
| Labeler / Manufacturer | Teva Pharmaceuticals USA, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA079011 |
| Dosage form / route | TABLET, FILM COATED, EXTENDED RELEASE · ORAL |
| Active ingredients | FLUVASTATIN SODIUM (80 mg/1) |
| Marketing started | 20160602 |
| Package count | 2 |
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