FDA NDC Directory · JSON-LD · Markdown
NDC 68462-504 · HUMAN PRESCRIPTION DRUG · TABLET
| Generic name | Norethindrone Acetate and Ethinyl Estradiol |
|---|---|
| Labeler / Manufacturer | Glenmark Pharmaceuticals Inc., USA |
| Marketing category | Abbreviated NDA (generic) · App ANDA209297 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | ETHINYL ESTRADIOL (.03 mg/1) NORETHINDRONE ACETATE (1.5 mg/1) |
| Marketing started | 20180605 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).