NDC 16729-371 – Tadalafil

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

Human Prescription Drug 4 recalls

Product NDC16729-371

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
April 3, 2020
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
16729-371-1030 TABLET, FILM COATED in 1 BOTTLE (16729-371-10)Apr 3, 2020
16729-371-16500 TABLET, FILM COATED in 1 BOTTLE (16729-371-16)Apr 29, 2020

Recalls mentioning this NDC

Other Tadalafil products