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
- 65862-149_6fb223b4-e6d7-4714-a9e0-5c05c5422c2a
- Product NDC
- 65862-149
- Form
- TABLET, FILM COATED
- Composition / generic term
- Finasteride
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20071030
- Source listing expiry
- 20271231
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 (65862-149-01) · 65862-149-01
- 500 TABLET, FILM COATED in 1 BOTTLE (65862-149-05) · 65862-149-05
- 30 TABLET, FILM COATED in 1 BOTTLE (65862-149-30) · 65862-149-30
- 90 TABLET, FILM COATED in 1 BOTTLE (65862-149-90) · 65862-149-90
Source and coverage
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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.
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