NDC 0093-5342 – Sildenafil

Sildenafil Citrate 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0093-5342

Product details

Brand name
Sildenafil
Generic name
Sildenafil
Labeler
Teva Pharmaceuticals USA, Inc.
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 (2)

Package NDCDescriptionSince
0093-5342-01100 TABLET, FILM COATED in 1 BOTTLE (0093-5342-01)Dec 11, 2017
0093-5342-5630 TABLET, FILM COATED in 1 BOTTLE (0093-5342-56)Dec 11, 2017

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