Allopurinol

Product NDC

71335-0599

11-digit product format

713350599

Labeler code

71335

Product ID

71335-0599_2fbf1174-1b16-4aac-a5d5-22165477fc1c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Allopurinol

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA071450

Marketing category

ANDA

Marketing start

1987-01-09

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