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
- 43598-390_47e5c3f0-f718-b400-c5f7-ba0057fdf6b1
- Product NDC
- 43598-390
- Form
- TABLET, FILM COATED
- Composition / generic term
- Finasteride
- Labeler
- Dr Reddys Laboratories Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140610
- Source listing expiry
- 20261231
Source-listed ingredients
- FINASTERIDE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (43598-390-30) · 43598-390-30
- 90 TABLET, FILM COATED in 1 BOTTLE (43598-390-90) · 43598-390-90
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 →