Allopurinol

Product NDC

68788-2115

11-digit product format

687882115

Labeler code

68788

Product ID

68788-2115_c0ebdd84-8118-44ab-aaf3-135f89b6895f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Allopurinol

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA071586

Marketing category

ANDA

Marketing start

2009-10-01

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