NDC 82009-079 – Tadalafil

Tadalafil 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82009-079

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Quallent Pharmaceuticals Health LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209654
Marketed since
July 19, 2023
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
82009-079-05500 TABLET in 1 BOTTLE (82009-079-05)Jul 19, 2023

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