# NALOXONE HYDROCHLORIDE AND PENTAZOCINE HYDROCHLORIDE
> **ANDA075523** · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARM INDS LTD · Approved 2000-03-17
## Drug
- **FDA Application Number:** 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
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=075523)
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*MORVS · CC0 1.0*