NDC 68071-2072 – Sildenafil

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

Human Prescription Drug

Product NDC68071-2072

Product details

Brand name
Sildenafil
Generic name
Sildenafil
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203814
Marketed since
January 3, 2014
Marketing end
October 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil →

Package NDC codes (4)

Package NDCDescriptionSince
68071-2072-110 TABLET, FILM COATED in 1 BOTTLE (68071-2072-1)Jan 24, 2017
68071-2072-228 TABLET, FILM COATED in 1 BOTTLE (68071-2072-2)Jan 24, 2017
68071-2072-44 TABLET, FILM COATED in 1 BOTTLE (68071-2072-4)Jan 24, 2017
68071-2072-520 TABLET, FILM COATED in 1 BOTTLE (68071-2072-5)Jan 24, 2017

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