United States · FDA National Drug Code directory
Finasteride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 35573-400_6752dcb1-091e-40a9-a6e2-069d543398a7
- Product NDC
- 35573-400
- Form
- TABLET, FILM COATED
- Composition / generic term
- Finasteride
- Labeler
- Burel Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180713
- Source listing expiry
- 20261231
Source-listed ingredients
- FINASTERIDE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, FILM COATED in 1 BOTTLE (35573-400-99) · 35573-400-99
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →