NDC 51655-487 – Tadalafil

Tadalafil 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC51655-487

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209167
Marketed since
November 25, 2020
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
51655-487-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-487-52)Nov 25, 2020

Recalls mentioning this NDC

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