NDC 50268-717 – Sildenafil

Sildenafil Citrate 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50268-717

Product details

Brand name
Sildenafil
Generic name
Sildenafil
Labeler
AvPAK
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202025
Marketed since
May 29, 2015
Listing expires
December 31, 2026
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil →

Package NDC codes (1)

Package NDCDescriptionSince
50268-717-1550 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-717-15) / 1 TABLET in 1 BLISTER PACK (50268-717-11)May 29, 2015

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