NDC 78206-152 – Propecia

Finasteride 1 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC78206-152

Product details

Brand name
Propecia
Generic name
finasteride
Labeler
Organon LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA020788
Marketed since
June 1, 2021
Listing expires
December 31, 2026
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Propecia →

Package NDC codes (2)

Package NDCDescriptionSince
78206-152-0130 TABLET, FILM COATED in 1 BOTTLE (78206-152-01)Jun 1, 2021
78206-152-0290 TABLET, FILM COATED in 1 BOTTLE (78206-152-02)Jun 1, 2021