Naltrexone Hydrochloride
NDC 53401-023, Naltrexone Hydrochloride, tablet, film coated, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 53401-023
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- 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/53401-023 \ -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 |
|---|---|---|
| 53401-023-30 | 53401002330 | 30 TABLET, FILM COATED in 1 BOTTLE (53401-023-30) |
| 53401-023-31 | 53401002331 | 600 TABLET, FILM COATED in 1 BOTTLE (53401-023-31) |
| 53401-023-53 | 53401002353 | 60 TABLET, FILM COATED in 1 BOTTLE (53401-023-53) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/57e8b767-54c2-dfa3-e063-6394a90ae6c2
Use it
Look up 53401-023 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/53401-023 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 53401-023. 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.