NDC 71335-1638 – Sildenafil

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

Human Prescription Drug

Product NDC71335-1638

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
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil →

Package NDC codes (9)

Package NDCDescriptionSince
71335-1638-110 TABLET, FILM COATED in 1 BOTTLE (71335-1638-1)Jan 3, 2014
71335-1638-230 TABLET, FILM COATED in 1 BOTTLE (71335-1638-2)Jan 3, 2014
71335-1638-37 TABLET, FILM COATED in 1 BOTTLE (71335-1638-3)Jan 3, 2014
71335-1638-490 TABLET, FILM COATED in 1 BOTTLE (71335-1638-4)Jan 3, 2014
71335-1638-560 TABLET, FILM COATED in 1 BOTTLE (71335-1638-5)Jan 3, 2014
71335-1638-620 TABLET, FILM COATED in 1 BOTTLE (71335-1638-6)Jan 3, 2014
71335-1638-7270 TABLET, FILM COATED in 1 BOTTLE (71335-1638-7)Jan 3, 2014
71335-1638-815 TABLET, FILM COATED in 1 BOTTLE (71335-1638-8)Jan 3, 2014
71335-1638-912 TABLET, FILM COATED in 1 BOTTLE (71335-1638-9)Jan 3, 2014

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