NDC 68382-896 – Tadalafil

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

Human Prescription Drug

Product NDC68382-896

Product details

Brand name
Tadalafil
Generic name
Tadalafil
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206693
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 (6)

Package NDCDescriptionSince
68382-896-01100 TABLET, FILM COATED in 1 BOTTLE (68382-896-01)Mar 27, 2019
68382-896-05500 TABLET, FILM COATED in 1 BOTTLE (68382-896-05)Mar 27, 2019
68382-896-0630 TABLET, FILM COATED in 1 BOTTLE (68382-896-06)Mar 27, 2019
68382-896-101000 TABLET, FILM COATED in 1 BOTTLE (68382-896-10)Mar 27, 2019
68382-896-1690 TABLET, FILM COATED in 1 BOTTLE (68382-896-16)Mar 27, 2019
68382-896-992 BLISTER PACK in 1 CARTON (68382-896-99) / 15 TABLET, FILM COATED in 1 BLISTER PACKMar 27, 2019

Other Tadalafil products