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
- 71335-1530_7b1f267c-70e7-4d31-8389-c4a59ccd727b
- Product NDC
- 71335-1530
- Form
- TABLET, FILM COATED
- Composition / generic term
- Finasteride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20071030
- Source listing expiry
- 20261231
Source-listed ingredients
- FINASTERIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-1530-1) · 71335-1530-1
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1530-2) · 71335-1530-2
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1530-3) · 71335-1530-3
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1530-4) · 71335-1530-4
- 500 TABLET, FILM COATED in 1 BOTTLE (71335-1530-5) · 71335-1530-5
- 180 TABLET, FILM COATED in 1 BOTTLE (71335-1530-6) · 71335-1530-6
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 →