Allopurinol

Product NDC

70518-0555

11-digit product format

705180555

Labeler code

70518

Product ID

70518-0555_85b72537-d447-7821-e053-2a91aa0a509c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Allopurinol

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

NDA018832

Marketing category

NDA

Marketing start

2017-05-25

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

2020-12-31

Current FDA listing

Historical FDA.report record