NDC 71335-2583 – Tadalafil

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

Human Prescription Drug

Product NDC71335-2583

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209250
Marketed since
March 26, 2019
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (8)

Package NDCDescriptionSince
71335-2583-130 TABLET, FILM COATED in 1 BOTTLE (71335-2583-1)Apr 3, 2025
71335-2583-210 TABLET, FILM COATED in 1 BOTTLE (71335-2583-2)Apr 3, 2025
71335-2583-390 TABLET, FILM COATED in 1 BOTTLE (71335-2583-3)Apr 3, 2025
71335-2583-45 TABLET, FILM COATED in 1 BOTTLE (71335-2583-4)Apr 3, 2025
71335-2583-560 TABLET, FILM COATED in 1 BOTTLE (71335-2583-5)Apr 3, 2025
71335-2583-620 TABLET, FILM COATED in 1 BOTTLE (71335-2583-6)Apr 3, 2025
71335-2583-715 TABLET, FILM COATED in 1 BOTTLE (71335-2583-7)Apr 3, 2025
71335-2583-8100 TABLET, FILM COATED in 1 BOTTLE (71335-2583-8)Apr 3, 2025

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