NDC 68645-541 – Finasteride

Finasteride 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68645-541

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Legacy Pharmaceutical Packaging, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090061
Marketed since
June 13, 2015
Listing expires
December 31, 2027
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (1)

Package NDCDescriptionSince
68645-541-5430 TABLET, FILM COATED in 1 BOTTLE (68645-541-54)Jun 13, 2015

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