NDC 71335-1649 – Sildenafil

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

Human Prescription Drug

Product NDC71335-1649

Product details

Brand name
Sildenafil
Generic name
Sildenafil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203623
Marketed since
November 26, 2014
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1649-050 TABLET, FILM COATED in 1 BOTTLE (71335-1649-0)Mar 1, 2022
71335-1649-110 TABLET, FILM COATED in 1 BOTTLE (71335-1649-1)Jul 9, 2020
71335-1649-230 TABLET, FILM COATED in 1 BOTTLE (71335-1649-2)Jun 24, 2020
71335-1649-37 TABLET, FILM COATED in 1 BOTTLE (71335-1649-3)May 10, 2021
71335-1649-490 TABLET, FILM COATED in 1 BOTTLE (71335-1649-4)Jun 23, 2020
71335-1649-560 TABLET, FILM COATED in 1 BOTTLE (71335-1649-5)Mar 31, 2021
71335-1649-620 TABLET, FILM COATED in 1 BOTTLE (71335-1649-6)Aug 13, 2020
71335-1649-7270 TABLET, FILM COATED in 1 BOTTLE (71335-1649-7)May 30, 2024
71335-1649-815 TABLET, FILM COATED in 1 BOTTLE (71335-1649-8)Jul 12, 2021
71335-1649-912 TABLET, FILM COATED in 1 BOTTLE (71335-1649-9)May 30, 2024

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