NDC 72603-784 – Tadalafil

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

Human Prescription Drug

Product NDC72603-784

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
NorthStar Rx, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211298
Marketed since
August 3, 2026
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
72603-784-011000 TABLET, FILM COATED in 1 BOTTLE (72603-784-01)Aug 3, 2026

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