FDA NDC Directory · JSON-LD · Markdown
NDC 50228-462 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE
| Generic name | PREGABALIN |
|---|---|
| Labeler / Manufacturer | ScieGen Pharmaceuticals, INC. |
| Marketing category | Abbreviated NDA (generic) · App ANDA215675 |
| Dosage form / route | TABLET, FILM COATED, EXTENDED RELEASE · ORAL |
| Active ingredients | PREGABALIN (82.5 mg/1) |
| Marketing started | 20220914 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).