Allopurinol

Product NDC

70518-0429

11-digit product format

705180429

Labeler code

70518

Product ID

70518-0429_85002c9f-660e-1c48-e053-2a91aa0ae920

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Allopurinol

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA018877

Marketing category

NDA

Marketing start

2017-04-17

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

2020-12-31

Current FDA listing

Historical FDA.report record