NDC 68071-2553 – Tadalafil

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

Human Prescription Drug

Product NDC68071-2553

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209167
Marketed since
March 27, 2019
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
68071-2553-330 TABLET, FILM COATED in 1 BOTTLE (68071-2553-3)Oct 25, 2021

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