NDC 71205-088 – Sildenafil

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

Human Prescription Drug

Product NDC71205-088

Product details

Brand name
Sildenafil
Generic name
Sildenafil
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077342
Marketed since
December 11, 2017
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil →

Package NDC codes (6)

Package NDCDescriptionSince
71205-088-1010 TABLET, FILM COATED in 1 BOTTLE (71205-088-10)Aug 1, 2018
71205-088-2020 TABLET, FILM COATED in 1 BOTTLE (71205-088-20)Apr 21, 2021
71205-088-3030 TABLET, FILM COATED in 1 BOTTLE (71205-088-30)Aug 1, 2018
71205-088-5050 TABLET, FILM COATED in 1 BOTTLE (71205-088-50)Aug 1, 2018
71205-088-6060 TABLET, FILM COATED in 1 BOTTLE (71205-088-60)Aug 1, 2018
71205-088-9090 TABLET, FILM COATED in 1 BOTTLE (71205-088-90)Aug 1, 2018

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