NDC 50090-7390 – Tadalafil

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

Human Prescription Drug

Product NDC50090-7390

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208934
Marketed since
February 19, 2020
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (2)

Package NDCDescriptionSince
50090-7390-090 TABLET, FILM COATED in 1 BOTTLE (50090-7390-0)Oct 23, 2024
50090-7390-130 TABLET, FILM COATED in 1 BOTTLE (50090-7390-1)Oct 23, 2024

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