NDC 60687-428 – Finasteride

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

Human Prescription Drug

Product NDC60687-428

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078341
Marketed since
September 9, 2019
Listing expires
December 31, 2026
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (2)

Package NDCDescriptionSince
60687-428-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-428-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-428-11)Sep 9, 2019
60687-428-6550 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-428-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-428-11)Jan 20, 2020

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