Finasteride
NDC 68071-3744, Finasteride, tablet, coated, from NuCare Pharmaceuticals, Inc..
- Product NDC
- 68071-3744
- Status
- Listed
- Labeler
- NuCare Pharmaceuticals, Inc.
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207750
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3744 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FINASTERIDE1 mg/1
Pharmacologic classes
5-alpha Reductase Inhibitor [EPC]; 5-alpha Reductase Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68071-3744-6 | 68071374406 | 60 TABLET, COATED in 1 BOTTLE (68071-3744-6) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/291a2037-2b4f-a2fe-e063-6294a90a1e9a
Use it
Look up 68071-3744 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3744 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68071-3744. 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.