← FDA Drug Approvals (Drugs@FDA)
LUNELLE
NDA · New Drug Application · Sponsor: PHARMACIA AND UPJOHN · Approved 2000-10-05
Drug application
- FDA Application #
NDA020874
- Application type
- New Drug Application
- Brand name
- LUNELLE
- Generic name
- Estradiol Cypionate
- Active ingredients
- ESTRADIOL CYPIONATE; MEDROXYPROGESTERONE ACETATE
- Dosage form
- INJECTABLE
- Route
- INTRAMUSCULAR
- Marketing status
- Discontinued
- Sponsor
- PHARMACIA AND UPJOHN
- First approval
- 2000-10-05
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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