NDC 71335-3049 – Sildenafil Citrate

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

Human Prescription Drug

Product NDC71335-3049

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 (10)

Package NDCDescriptionSince
71335-3049-015 TABLET, FILM COATED in 1 BOTTLE (71335-3049-0)Mar 9, 2026
71335-3049-110 TABLET, FILM COATED in 1 BOTTLE (71335-3049-1)Mar 9, 2026
71335-3049-25 TABLET, FILM COATED in 1 BOTTLE (71335-3049-2)Mar 9, 2026
71335-3049-330 TABLET, FILM COATED in 1 BOTTLE (71335-3049-3)Mar 9, 2026
71335-3049-42 TABLET, FILM COATED in 1 BOTTLE (71335-3049-4)Mar 9, 2026
71335-3049-56 TABLET, FILM COATED in 1 BOTTLE (71335-3049-5)Mar 9, 2026
71335-3049-620 TABLET, FILM COATED in 1 BOTTLE (71335-3049-6)Mar 9, 2026
71335-3049-74 TABLET, FILM COATED in 1 BOTTLE (71335-3049-7)Mar 9, 2026
71335-3049-890 TABLET, FILM COATED in 1 BOTTLE (71335-3049-8)Mar 9, 2026
71335-3049-960 TABLET, FILM COATED in 1 BOTTLE (71335-3049-9)Mar 9, 2026

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