FDA NDC Directory · JSON-LD · Markdown
NDC 59651-366 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION
| Labeler / Manufacturer | Aurobindo Pharma Limited |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA213899 |
| Dosage form / route | POWDER, FOR SOLUTION · ORAL |
| Active ingredients | VIGABATRIN (500 mg/1) |
| Marketing started | 20210929 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).