NDC 71205-502 – Tadalafil

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

Human Prescription Drug

Product NDC71205-502

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209167
Marketed since
April 3, 2020
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
71205-502-1010 TABLET, FILM COATED in 1 BOTTLE (71205-502-10)Nov 11, 2020
71205-502-1515 TABLET, FILM COATED in 1 BOTTLE (71205-502-15)Jun 10, 2021
71205-502-3030 TABLET, FILM COATED in 1 BOTTLE (71205-502-30)Nov 11, 2020
71205-502-6060 TABLET, FILM COATED in 1 BOTTLE (71205-502-60)Nov 11, 2020
71205-502-9090 TABLET, FILM COATED in 1 BOTTLE (71205-502-90)Nov 11, 2020

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