NDC 71205-509 – Sildenafil

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

Human Prescription Drug

Product NDC71205-509

Product details

Brand name
Sildenafil
Generic name
Sildenafil
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078380
Marketed since
May 31, 2013
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil →

Package NDC codes (3)

Package NDCDescriptionSince
71205-509-3030 TABLET, FILM COATED in 1 BOTTLE (71205-509-30)Nov 24, 2020
71205-509-6060 TABLET, FILM COATED in 1 BOTTLE (71205-509-60)Nov 24, 2020
71205-509-9090 TABLET, FILM COATED in 1 BOTTLE (71205-509-90)Nov 24, 2020

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