Naltrexone Hydrochloride
NDC 71335-0014, Naltrexone Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 71335-0014
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA091205
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0014 \ -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 |
|---|---|---|
| 71335-0014-1 | 71335001401 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0014-1) |
| 71335-0014-2 | 71335001402 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0014-2) |
| 71335-0014-3 | 71335001403 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0014-3) |
| 71335-0014-4 | 71335001404 | 45 TABLET, FILM COATED in 1 BOTTLE (71335-0014-4) |
| 71335-0014-5 | 71335001405 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0014-5) |
| 71335-0014-6 | 71335001406 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-0014-6) |
| 71335-0014-7 | 71335001407 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0014-7) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/fa0b0881-97f3-4ca2-bc15-0954293081db
Use it
Look up 71335-0014 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0014 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71335-0014. 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.