NDC 16729-369 – Tadalafil

Tadalafil 2.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 4 recalls

Product NDC16729-369

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Accord Healthcare Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209167
Marketed since
March 27, 2019
Listing expires
December 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (2)

Package NDCDescriptionSince
16729-369-1030 TABLET, FILM COATED in 1 BOTTLE (16729-369-10)Mar 27, 2019
16729-369-16500 TABLET, FILM COATED in 1 BOTTLE (16729-369-16)May 5, 2020

Recalls mentioning this NDC

Other Tadalafil products