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: 76420-074_ead2d1fe-f89c-ee3a-e053-2995a90ac920
Product NDC: 76420-074
Form: TABLET, FILM COATED
Composition / generic term: Finasteride
Labeler: Asclemed USA, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20130701
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 (76420-074-30) · 76420-074-30

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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