← FDA Drug Approvals (Drugs@FDA)
JUNEL FE 1/20
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: BARR · Approved 2003-09-18
Drug application
- FDA Application #
ANDA076081
- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- JUNEL FE 1/20
- Generic name
- NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE
- Active ingredients
- ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
- Dosage form
- TABLET
- Route
- ORAL-28
- Marketing status
- Prescription
- Sponsor
- BARR
- Manufacturer
- Teva Pharmaceuticals USA, Inc.
- First approval
- 2003-09-18
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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