Finasteride
NDC 82009-061, Finasteride, tablet, film coated, from QUALLENT PHARMACEUTICALS HEALTH LLC.
- Product NDC
- 82009-061
- Status
- Listed
- Labeler
- QUALLENT PHARMACEUTICALS HEALTH LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078341
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/82009-061 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- FINASTERIDE5 mg/1
Pharmacologic classes
5-alpha Reductase Inhibitor [EPC]; 5-alpha Reductase Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 82009-061-05 | 82009006105 | 500 TABLET, FILM COATED in 1 BOTTLE (82009-061-05) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5efc695c-d9fd-4892-a63f-a35cceb8d3c7NADAC price for package 82009006105
GET /v1/drugs/nadac/82009006105
Use it
Look up 82009-061 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/82009-061 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 82009-061. 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.