NDC 71335-1088 – Sildenafil

Sildenafil Citrate 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1088

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, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1088-015 TABLET, FILM COATED in 1 BOTTLE (71335-1088-0)Feb 9, 2022
71335-1088-110 TABLET, FILM COATED in 1 BOTTLE (71335-1088-1)Feb 9, 2022
71335-1088-25 TABLET, FILM COATED in 1 BOTTLE (71335-1088-2)Feb 9, 2022
71335-1088-330 TABLET, FILM COATED in 1 BOTTLE (71335-1088-3)Feb 9, 2022
71335-1088-42 TABLET, FILM COATED in 1 BOTTLE (71335-1088-4)Feb 9, 2022
71335-1088-56 TABLET, FILM COATED in 1 BOTTLE (71335-1088-5)Feb 9, 2022
71335-1088-620 TABLET, FILM COATED in 1 BOTTLE (71335-1088-6)Feb 9, 2022
71335-1088-74 TABLET, FILM COATED in 1 BOTTLE (71335-1088-7)Feb 9, 2022
71335-1088-890 TABLET, FILM COATED in 1 BOTTLE (71335-1088-8)Feb 9, 2022
71335-1088-960 TABLET, FILM COATED in 1 BOTTLE (71335-1088-9)Feb 9, 2022

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