NDC 63629-5029 – Sildenafil

Sildenafil Citrate 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-5029

Product details

Brand name
Sildenafil
Generic name
Sildenafil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202025
Marketed since
November 8, 2012
Listing expires
December 31, 2027
Pharmacologic class
Phosphodiesterase 5 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sildenafil →

Package NDC codes (10)

Package NDCDescriptionSince
63629-5029-050 TABLET in 1 BOTTLE (63629-5029-0)Aug 6, 2026
63629-5029-110 TABLET in 1 BOTTLE (63629-5029-1)Aug 21, 2013
63629-5029-230 TABLET in 1 BOTTLE (63629-5029-2)Jun 6, 2013
63629-5029-37 TABLET in 1 BOTTLE (63629-5029-3)Aug 2, 2013
63629-5029-490 TABLET in 1 BOTTLE (63629-5029-4)May 8, 2014
63629-5029-560 TABLET in 1 BOTTLE (63629-5029-5)Mar 28, 2018
63629-5029-620 TABLET in 1 BOTTLE (63629-5029-6)Mar 24, 2016
63629-5029-7270 TABLET in 1 BOTTLE (63629-5029-7)Aug 6, 2026
63629-5029-815 TABLET in 1 BOTTLE (63629-5029-8)Aug 6, 2026
63629-5029-912 TABLET in 1 BOTTLE (63629-5029-9)Oct 25, 2017

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