NDC 71335-3111 – Sildenafil Citrate

Sildenafil Citrate 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-3111

Product details

Brand name
Sildenafil Citrate
Generic name
Sildenafil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091448
Marketed since
June 11, 2018
Listing expires
December 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil Citrate →

Package NDC codes (8)

Package NDCDescriptionSince
71335-3111-130 TABLET, FILM COATED in 1 BOTTLE (71335-3111-1)Mar 30, 2026
71335-3111-210 TABLET, FILM COATED in 1 BOTTLE (71335-3111-2)Mar 30, 2026
71335-3111-315 TABLET, FILM COATED in 1 BOTTLE (71335-3111-3)Mar 30, 2026
71335-3111-490 TABLET, FILM COATED in 1 BOTTLE (71335-3111-4)Mar 30, 2026
71335-3111-560 TABLET, FILM COATED in 1 BOTTLE (71335-3111-5)Mar 30, 2026
71335-3111-620 TABLET, FILM COATED in 1 BOTTLE (71335-3111-6)Mar 30, 2026
71335-3111-77 TABLET, FILM COATED in 1 BOTTLE (71335-3111-7)Mar 30, 2026
71335-3111-840 TABLET, FILM COATED in 1 BOTTLE (71335-3111-8)Mar 30, 2026

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