Allopurinol

Product NDC

50742-135

11-digit product format

507420135

Labeler code

50742

Product ID

50742-135_457d1969-77ba-47c3-904e-95b1b3fa1db2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Allopurinol

Dosage form

TABLET

Route

ORAL

Labeler

Ingenus Pharmaceuticals LLC

Application

ANDA204467

Marketing category

ANDA

Marketing start

2016-08-08

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