NDC 71335-0969 – Sildenafil

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

Human Prescription Drug

Product NDC71335-0969

Product details

Brand name
Sildenafil
Generic name
Sildenafil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202023
Marketed since
June 28, 2018
Listing expires
December 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0969-015 TABLET, FILM COATED in 1 BOTTLE (71335-0969-0)Feb 7, 2019
71335-0969-110 TABLET, FILM COATED in 1 BOTTLE (71335-0969-1)Oct 18, 2018
71335-0969-25 TABLET, FILM COATED in 1 BOTTLE (71335-0969-2)Dec 21, 2018
71335-0969-330 TABLET, FILM COATED in 1 BOTTLE (71335-0969-3)Nov 5, 2018
71335-0969-42 TABLET, FILM COATED in 1 BOTTLE (71335-0969-4)Aug 19, 2026
71335-0969-56 TABLET, FILM COATED in 1 BOTTLE (71335-0969-5)Aug 19, 2026
71335-0969-620 TABLET, FILM COATED in 1 BOTTLE (71335-0969-6)Nov 28, 2018
71335-0969-74 TABLET, FILM COATED in 1 BOTTLE (71335-0969-7)Aug 19, 2026
71335-0969-890 TABLET, FILM COATED in 1 BOTTLE (71335-0969-8)Aug 19, 2026
71335-0969-960 TABLET, FILM COATED in 1 BOTTLE (71335-0969-9)Aug 19, 2026

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