NDC 63629-1307 – Sucralfate

Sucralfate 1 g/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-1307

Product details

Brand name
Sucralfate
Generic name
Sucralfate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA070848
Marketed since
November 11, 1996
Listing expires
December 31, 2026
Pharmacologic class
Aluminum Complex

Active ingredients

Uses, dosage, side effects and warnings for Sucralfate →

Package NDC codes (9)

Package NDCDescriptionSince
63629-1307-028 TABLET in 1 BOTTLE (63629-1307-0)Nov 8, 2022
63629-1307-1100 TABLET in 1 BOTTLE (63629-1307-1)Feb 5, 2007
63629-1307-260 TABLET in 1 BOTTLE (63629-1307-2)Apr 12, 2010
63629-1307-330 TABLET in 1 BOTTLE (63629-1307-3)Sep 19, 2008
63629-1307-420 TABLET in 1 BOTTLE (63629-1307-4)Oct 17, 2013
63629-1307-6150 TABLET in 1 BOTTLE (63629-1307-6)Nov 8, 2022
63629-1307-790 TABLET in 1 BOTTLE (63629-1307-7)Sep 13, 2010
63629-1307-840 TABLET in 1 BOTTLE (63629-1307-8)Feb 23, 2012
63629-1307-9120 TABLET in 1 BOTTLE (63629-1307-9)May 31, 2013

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