NDC 24979-729 – Tadalafil

Tadalafil 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC24979-729

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210420
Marketed since
April 7, 2024
Listing expires
December 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (2)

Package NDCDescriptionSince
24979-729-0630 TABLET, FILM COATED in 1 BOTTLE (24979-729-06)Apr 7, 2024
24979-729-69250 TABLET, FILM COATED in 1 BOTTLE (24979-729-69)Apr 7, 2024

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