NDC 52817-295 – Sildenafil Citrate

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

Human Prescription Drug

Product NDC52817-295

Product details

Brand name
Sildenafil Citrate
Generic name
Sildenafil
Labeler
TruPharma LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204883
Marketed since
August 1, 2016
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil Citrate →

Package NDC codes (2)

Package NDCDescriptionSince
52817-295-001000 TABLET, FILM COATED in 1 BOTTLE (52817-295-00)Aug 1, 2016
52817-295-9090 TABLET, FILM COATED in 1 BOTTLE (52817-295-90)Aug 1, 2016

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