Naltrexone Hydrochloride
NDC 42291-632, Naltrexone Hydrochloride, tablet, film coated, from AvKARE.
- Product NDC
- 42291-632
- Status
- Listed
- Labeler
- AvKARE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075274
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42291-632 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- NALTREXONE HYDROCHLORIDE50 mg/1
Pharmacologic classes
Opioid Antagonist [EPC]; Opioid Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42291-632-30 | 42291063230 | 30 TABLET, FILM COATED in 1 BOTTLE (42291-632-30) |
| 42291-632-60 | 42291063260 | 60 TABLET, FILM COATED in 1 BOTTLE (42291-632-60) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/21b43dab-015c-c82f-ba6e-27da0ec12fc5
Use it
Look up 42291-632 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42291-632 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42291-632. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.