← FDA Drug Approvals (Drugs@FDA)
LOESTRIN FE 1/20
NDA · New Drug Application · Sponsor: TEVA BRANDED PHARM · Approved 1973-04-30
Drug application
- FDA Application #
NDA017354
- Application type
- New Drug Application
- Brand name
- LOESTRIN FE 1/20
- Generic name
- Ethinyl Estradiol
- Active ingredients
- ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
- Dosage form
- TABLET
- Route
- ORAL-28
- Marketing status
- Discontinued
- Sponsor
- TEVA BRANDED PHARM
- First approval
- 1973-04-30
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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