FDA NDC Directory · JSON-LD · Markdown
NDC 59651-439 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Generic name | Estradiol |
|---|---|
| Labeler / Manufacturer | Aurobindo Pharma Limited |
| Marketing category | Abbreviated NDA (generic) · App ANDA216550 |
| Dosage form / route | TABLET, FILM COATED · VAGINAL |
| Active ingredients | ESTRADIOL HEMIHYDRATE (10 ug/1) |
| Marketing started | 20240802 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).