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NORETHINDRONE AND ETHINYL ESTRADIOL (7/14)
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: WATSON LABS · Approved 1991-09-24
Drug application
- FDA Application #
ANDA071042- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- NORETHINDRONE AND ETHINYL ESTRADIOL (7/14)
- Generic name
- Ethinyl Estradiol
- Active ingredients
- ETHINYL ESTRADIOL; NORETHINDRONE
- Dosage form
- TABLET
- Route
- ORAL-28
- Marketing status
- Discontinued
- Sponsor
- WATSON LABS
- First approval
- 1991-09-24
Source
- Authoritative
- Drugs@FDA application overview
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