NDC 71335-1255 – Tadalafil

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

Human Prescription Drug

Product NDC71335-1255

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208934
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 (7)

Package NDCDescriptionSince
71335-1255-130 TABLET, FILM COATED in 1 BOTTLE (71335-1255-1)Jun 20, 2019
71335-1255-210 TABLET, FILM COATED in 1 BOTTLE (71335-1255-2)Jun 21, 2019
71335-1255-390 TABLET, FILM COATED in 1 BOTTLE (71335-1255-3)May 17, 2024
71335-1255-45 TABLET, FILM COATED in 1 BOTTLE (71335-1255-4)May 17, 2024
71335-1255-560 TABLET, FILM COATED in 1 BOTTLE (71335-1255-5)May 17, 2024
71335-1255-620 TABLET, FILM COATED in 1 BOTTLE (71335-1255-6)May 17, 2024
71335-1255-715 TABLET, FILM COATED in 1 BOTTLE (71335-1255-7)May 17, 2024

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