NDC 35573-400 – Finasteride

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

Human Prescription Drug

Product NDC35573-400

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Burel Pharmaceuticals, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203687
Marketed since
July 13, 2018
Listing expires
December 31, 2026
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (1)

Package NDCDescriptionSince
35573-400-991000 TABLET, FILM COATED in 1 BOTTLE (35573-400-99)Jul 13, 2018

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