NDC 71610-567 – Tadalafil

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

Human Prescription Drug

Product NDC71610-567

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209744
Marketed since
January 21, 2021
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (4)

Package NDCDescriptionSince
71610-567-044 TABLET, FILM COATED in 1 BOTTLE (71610-567-04)Jun 10, 2021
71610-567-1212 TABLET, FILM COATED in 1 BOTTLE (71610-567-12)Jun 10, 2021
71610-567-31600 TABLET, FILM COATED in 1 BOTTLE (71610-567-31)Mar 22, 2024
71610-567-5218 TABLET, FILM COATED in 1 BOTTLE (71610-567-52)Feb 5, 2025

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