NDC 72303-0825 – Tadalafil

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

Human Prescription Drug

Product NDC72303-0825

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
HEC Pharm USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211335
Marketed since
March 27, 2019
Listing expires
December 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (1)

Package NDCDescriptionSince
72303-0825-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72303-0825-1)Mar 27, 2019

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