NDC 50090-8039 – Tadalafil

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

Human Prescription Drug

Product NDC50090-8039

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211298
Marketed since
February 15, 2026
Listing expires
December 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (3)

Package NDCDescriptionSince
50090-8039-030 TABLET, FILM COATED in 1 BOTTLE (50090-8039-0)Aug 26, 2026
50090-8039-110 TABLET, FILM COATED in 1 BOTTLE (50090-8039-1)Aug 26, 2026
50090-8039-290 TABLET, FILM COATED in 1 BOTTLE (50090-8039-2)Aug 26, 2026

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