NDC 71713-099 – Finasteride

Finasteride 1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71713-099

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Thirty Madison Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207750
Marketed since
March 22, 2021
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
71713-099-9090 TABLET in 1 CONTAINER (71713-099-90)Mar 22, 2021

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