Allopurinol

Product NDC

70518-0190

11-digit product format

705180190

Labeler code

70518

Product ID

70518-0190_82cdda2a-91d0-4ef6-e053-2991aa0a2edf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

allopurinol

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA075798

Marketing category

ANDA

Marketing start

2017-01-31

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