NDC 63629-1781 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-1781

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA018877
Marketed since
April 6, 2009
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (5)

Package NDCDescriptionSince
63629-1781-130 TABLET in 1 BOTTLE (63629-1781-1)Apr 6, 2009
63629-1781-260 TABLET in 1 BOTTLE (63629-1781-2)Apr 6, 2009
63629-1781-3100 TABLET in 1 BOTTLE (63629-1781-3)Apr 6, 2009
63629-1781-490 TABLET in 1 BOTTLE (63629-1781-4)Apr 6, 2009
63629-1781-520 TABLET in 1 BOTTLE (63629-1781-5)Apr 6, 2009

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