NDC 68788-8153 – Tadalafil

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

Human Prescription Drug 1 recall

Product NDC68788-8153

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209167
Marketed since
March 14, 2022
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
68788-8153-77 TABLET, FILM COATED in 1 BOTTLE (68788-8153-7)Mar 14, 2022

Recalls mentioning this NDC

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