← FDA Drug Approvals (Drugs@FDA)
GILDESS FE 1/20
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: PH HEALTH · Approved 2005-05-20
Drug application
- FDA Application #
ANDA077077
- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- GILDESS FE 1/20
- Generic name
- Ethinyl Estradiol
- Active ingredients
- ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
- Dosage form
- TABLET
- Route
- ORAL-28
- Marketing status
- Discontinued
- Sponsor
- PH HEALTH
- First approval
- 2005-05-20
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown