NDC 71335-1005 – Sildenafil

Sildenafil Citrate 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1005

Product details

Brand name
Sildenafil
Generic name
Sildenafil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203814
Marketed since
January 3, 2014
Marketing end
October 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil →

Package NDC codes (9)

Package NDCDescriptionSince
71335-1005-110 TABLET, FILM COATED in 1 BOTTLE (71335-1005-1)Oct 14, 2016
71335-1005-230 TABLET, FILM COATED in 1 BOTTLE (71335-1005-2)Oct 14, 2016
71335-1005-37 TABLET, FILM COATED in 1 BOTTLE (71335-1005-3)Oct 14, 2016
71335-1005-490 TABLET, FILM COATED in 1 BOTTLE (71335-1005-4)Oct 14, 2016
71335-1005-560 TABLET, FILM COATED in 1 BOTTLE (71335-1005-5)Oct 14, 2016
71335-1005-620 TABLET, FILM COATED in 1 BOTTLE (71335-1005-6)Oct 14, 2016
71335-1005-7270 TABLET, FILM COATED in 1 BOTTLE (71335-1005-7)Oct 14, 2016
71335-1005-815 TABLET, FILM COATED in 1 BOTTLE (71335-1005-8)Oct 14, 2016
71335-1005-912 TABLET, FILM COATED in 1 BOTTLE (71335-1005-9)Oct 14, 2016

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