United States · FDA National Drug Code directory
PROSCAR
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
- 78206-153_979b0a0c-7868-4ec1-8887-f2b7e43f4326
- Product NDC
- 78206-153
- Form
- TABLET, FILM COATED
- Composition / generic term
- FINASTERIDE
- Labeler
- Organon LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20210601
- Source listing expiry
- 20271231
Source-listed ingredients
- FINASTERIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (78206-153-01) · 78206-153-01
- 100 TABLET, FILM COATED in 1 BOTTLE (78206-153-02) · 78206-153-02
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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