NDC 71335-1587 – Tadalafil

Tadalafil 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1587

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209167
Marketed since
March 27, 2019
Listing expires
December 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (8)

Package NDCDescriptionSince
71335-1587-130 TABLET, FILM COATED in 1 BOTTLE (71335-1587-1)Apr 30, 2020
71335-1587-210 TABLET, FILM COATED in 1 BOTTLE (71335-1587-2)Jun 16, 2020
71335-1587-390 TABLET, FILM COATED in 1 BOTTLE (71335-1587-3)Jul 22, 2020
71335-1587-45 TABLET, FILM COATED in 1 BOTTLE (71335-1587-4)Sep 11, 2020
71335-1587-560 TABLET, FILM COATED in 1 BOTTLE (71335-1587-5)Aug 14, 2020
71335-1587-620 TABLET, FILM COATED in 1 BOTTLE (71335-1587-6)Oct 31, 2024
71335-1587-715 TABLET, FILM COATED in 1 BOTTLE (71335-1587-7)Jun 23, 2020
71335-1587-8100 TABLET, FILM COATED in 1 BOTTLE (71335-1587-8)Jun 23, 2020

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