NDC 51655-063 – Tadalafil

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

Human Prescription Drug

Product NDC51655-063

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206693
Marketed since
September 27, 2022
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
51655-063-5415 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-063-54)Sep 27, 2022
51655-063-876 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-063-87)Sep 27, 2022

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