Drug Atlas

NDC 68382-899 – Tadalafil

Tadalafil 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68382-899

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

Tadalafil 20 mg/1

Uses, dosage, side effects and warnings for Tadalafil →

Package NDC codes (6)

Package NDC	Description	Since
68382-899-01	100 TABLET, FILM COATED in 1 BOTTLE (68382-899-01)	Mar 27, 2019
68382-899-05	500 TABLET, FILM COATED in 1 BOTTLE (68382-899-05)	Mar 27, 2019
68382-899-06	30 TABLET, FILM COATED in 1 BOTTLE (68382-899-06)	Mar 27, 2019
68382-899-10	1000 TABLET, FILM COATED in 1 BOTTLE (68382-899-10)	Mar 27, 2019
68382-899-16	90 TABLET, FILM COATED in 1 BOTTLE (68382-899-16)	Mar 27, 2019
68382-899-99	2 BLISTER PACK in 1 CARTON (68382-899-99) / 15 TABLET, FILM COATED in 1 BLISTER PACK	Mar 27, 2019

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