Allopurinol

Product NDC

55154-2056

11-digit product format

551542056

Labeler code

55154

Product ID

55154-2056_b9c6e647-d23c-4026-abc2-49a555b4f3d6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Allopurinol

Dosage form

TABLET

Route

ORAL

Labeler

Cardinal Health

Application

NDA018832

Marketing category

NDA

Marketing start

2009-03-11

Marketing end

0000-00-00

Substance

ALLOPURINOL

Active strength

300 mg/1

Pharmacologic classes

Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record