NDC 71335-1028 – Sildenafil

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

Human Prescription Drug

Product NDC71335-1028

Product details

Brand name
Sildenafil
Generic name
Sildenafil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202659
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 →

Package NDC codes (8)

Package NDCDescriptionSince
71335-1028-130 TABLET, FILM COATED in 1 BOTTLE (71335-1028-1)Jul 12, 2019
71335-1028-210 TABLET, FILM COATED in 1 BOTTLE (71335-1028-2)Dec 13, 2018
71335-1028-315 TABLET, FILM COATED in 1 BOTTLE (71335-1028-3)Jul 11, 2019
71335-1028-490 TABLET, FILM COATED in 1 BOTTLE (71335-1028-4)Feb 9, 2021
71335-1028-560 TABLET, FILM COATED in 1 BOTTLE (71335-1028-5)Nov 21, 2019
71335-1028-620 TABLET, FILM COATED in 1 BOTTLE (71335-1028-6)Sep 7, 2021
71335-1028-77 TABLET, FILM COATED in 1 BOTTLE (71335-1028-7)Nov 21, 2019
71335-1028-840 TABLET, FILM COATED in 1 BOTTLE (71335-1028-8)Nov 21, 2019

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