← FDA Drug Approvals (Drugs@FDA)
NALTREXONE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: ELITE LABS · Approved 1999-05-26
Drug application
- FDA Application #
ANDA075274
- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- NALTREXONE HYDROCHLORIDE
- Generic name
- NALTREXONE HYDROCHLORIDE
- Active ingredients
- NALTREXONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- ELITE LABS
- Manufacturer
- Elite Laboratories, Inc.
- First approval
- 1999-05-26
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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