NDC 71205-269 – Tadalafil

Tadalafil 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71205-269

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
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 (3)

Package NDCDescriptionSince
71205-269-3030 TABLET, FILM COATED in 1 BOTTLE (71205-269-30)May 1, 2019
71205-269-6060 TABLET, FILM COATED in 1 BOTTLE (71205-269-60)May 1, 2019
71205-269-9090 TABLET, FILM COATED in 1 BOTTLE (71205-269-90)May 1, 2019

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