← FDA Drug Approvals (Drugs@FDA)
NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARM INDS LTD · Approved 2000-03-17
Drug application
- FDA Application #
ANDA075523- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE
- Generic name
- PENTAZOCINE AND NALOXONE
- Active ingredients
- NALOXONE HYDROCHLORIDE; PENTAZOCINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- SUN PHARM INDS LTD
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- First approval
- 2000-03-17
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown