NDC 71610-581 – Tadalafil

Tadalafil 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71610-581

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 (5)

Package NDCDescriptionSince
71610-581-044 TABLET, FILM COATED in 1 BOTTLE (71610-581-04)Jul 12, 2021
71610-581-066 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-581-06)Feb 1, 2023
71610-581-1212 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-581-12)Jul 12, 2021
71610-581-391440 TABLET, FILM COATED in 1 BOTTLE (71610-581-39)Apr 3, 2024
71610-581-5218 TABLET, FILM COATED in 1 BOTTLE (71610-581-52)Sep 5, 2024

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