NDC 71205-220 – Sildenafil

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

Human Prescription Drug

Product NDC71205-220

Product details

Brand name
Sildenafil
Generic name
Sildenafil
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203962
Marketed since
June 11, 2018
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
71205-220-1010 TABLET, FILM COATED in 1 BOTTLE (71205-220-10)Feb 1, 2019
71205-220-2020 TABLET, FILM COATED in 1 BOTTLE (71205-220-20)Feb 1, 2019
71205-220-3030 TABLET, FILM COATED in 1 BOTTLE (71205-220-30)Feb 1, 2019
71205-220-5050 TABLET, FILM COATED in 1 BOTTLE (71205-220-50)Feb 1, 2019
71205-220-6060 TABLET, FILM COATED in 1 BOTTLE (71205-220-60)Feb 1, 2019
71205-220-9090 TABLET, FILM COATED in 1 BOTTLE (71205-220-90)Feb 1, 2019

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