NDC 72865-108 – Tadalafil

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

Human Prescription Drug

Product NDC72865-108

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
XLCare Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209908
Marketed since
December 10, 2024
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (1)

Package NDCDescriptionSince
72865-108-3030 TABLET, FILM COATED in 1 BOTTLE (72865-108-30)Dec 10, 2024

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