NDC 47335-010 – Tadalafil

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

Human Prescription Drug

Product NDC47335-010

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 (2)

Package NDCDescriptionSince
47335-010-642 BLISTER PACK in 1 CARTON (47335-010-64) / 15 TABLET, FILM COATED in 1 BLISTER PACKMar 26, 2019
47335-010-8330 TABLET, FILM COATED in 1 BOTTLE (47335-010-83)Mar 26, 2019

Other Tadalafil products