NDC 70771-1048 – Vardenafil

Vardenafil Hydrochloride Trihydrate 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70771-1048

Product details

Brand name
Vardenafil
Generic name
Vardenafil
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208960
Marketed since
November 1, 2018
Listing expires
December 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Vardenafil →

Package NDC codes (3)

Package NDCDescriptionSince
70771-1048-1100 TABLET, FILM COATED in 1 BOTTLE (70771-1048-1)Nov 1, 2018
70771-1048-330 TABLET, FILM COATED in 1 BOTTLE (70771-1048-3)Nov 1, 2018
70771-1048-990 TABLET, FILM COATED in 1 BOTTLE (70771-1048-9)Nov 1, 2018

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