NDC 47335-012 – Tadalafil

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

Human Prescription Drug

Product NDC47335-012

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Sun Pharmaceutical Industries, Inc.
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 (1)

Package NDCDescriptionSince
47335-012-8330 TABLET, FILM COATED in 1 BOTTLE (47335-012-83)Mar 26, 2019

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