Allopurinol

Product NDC

68788-9832

11-digit product format

687889832

Labeler code

68788

Product ID

68788-9832_80f59cac-87cf-4c16-b5a4-ad0cc80ca3af

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Allopurinol

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA090637

Marketing category

ANDA

Marketing start

2012-06-04

Marketing end

0000-00-00

Substance

ALLOPURINOL

Active strength

100 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