Allopurinol

Product NDC

50090-0042

11-digit product format

500900042

Labeler code

50090

Product ID

50090-0042_e8e15b37-16b1-485d-9150-d870e8688026

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Allopurinol

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA078253

Marketing category

ANDA

Marketing start

2009-11-16

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

2021-12-31

Current FDA listing

Historical FDA.report record