← FDA Drug Approvals (Drugs@FDA)
ORNIDYL
NDA · New Drug Application · Sponsor: SANOFI AVENTIS US · Approved 1990-11-28
Drug application
- FDA Application #
NDA019879- Application type
- New Drug Application
- Brand name
- ORNIDYL
- Generic name
- Eflornithine Hydrochloride
- Active ingredients
- EFLORNITHINE HYDROCHLORIDE
- Dosage form
- INJECTABLE
- Route
- INJECTION
- Marketing status
- Discontinued
- Sponsor
- SANOFI AVENTIS US
- First approval
- 1990-11-28
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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