NDC 68382-897 – Tadalafil

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

Human Prescription Drug

Product NDC68382-897

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 (7)

Package NDCDescriptionSince
68382-897-01100 TABLET, FILM COATED in 1 BOTTLE (68382-897-01)Mar 27, 2019
68382-897-05500 TABLET, FILM COATED in 1 BOTTLE (68382-897-05)Mar 27, 2019
68382-897-0630 TABLET, FILM COATED in 1 BOTTLE (68382-897-06)Mar 27, 2019
68382-897-101000 TABLET, FILM COATED in 1 BOTTLE (68382-897-10)Mar 27, 2019
68382-897-1690 TABLET, FILM COATED in 1 BOTTLE (68382-897-16)Mar 27, 2019
68382-897-5010 TABLET, FILM COATED in 1 BOTTLE (68382-897-50)Mar 27, 2019
68382-897-992 BLISTER PACK in 1 CARTON (68382-897-99) / 15 TABLET, FILM COATED in 1 BLISTER PACKMar 27, 2019

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