Allopurinol

Product NDC

55700-035

11-digit product format

557000035

Labeler code

55700

Product ID

55700-035_f0c6c86e-57a9-426d-afd8-6ff02045d026

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

allopurinol

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA075798

Marketing category

ANDA

Marketing start

2003-06-27

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