NDC 0480-2309 – Tadalafil

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

Human Prescription Drug

Product NDC0480-2309

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Teva Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA205885
Marketed since
January 16, 2024
Marketing end
February 28, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (1)

Package NDCDescriptionSince
0480-2309-5630 TABLET, FILM COATED in 1 BOTTLE (0480-2309-56)Jan 16, 2024

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