Allopurinol

Basic Information

Product Name

Allopurinol

FDA Product Code

29300-349

Regulatory Information

NDC Product Code

29300-349

Application Number

ANDA211820

Marketing Category

C73584

Effective Date

February 9, 2024

Territorial Authority

USA

FDA Title

These highlights do not include all the information needed to use ALLOPURINOL TABLETS safely and effectively. See full prescribing information for ALLOPURINOL TABLETS.ALLOPURINOL tablets, for oral use. Initial U.S. Approval:1966

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

Active Ingredients

ALLOPURINOL

Quantity: 100 mg in 1 1

Code: 63CZ7GJN5I

Class Code: ACTIB

CROSCARMELLOSE SODIUM

Code: M28OL1HH48

Class Code: IACT

LACTOSE MONOHYDRATE

Code: EWQ57Q8I5X

Class Code: IACT

MAGNESIUM STEARATE

Code: 70097M6I30

Class Code: IACT

STARCH, CORN

Code: O8232NY3SJ

Class Code: IACT

POVIDONE K30

Code: U725QWY32X

Class Code: IACT

Active Moieties

Code: 63CZ7GJN5I

Allopurinol

Basic Information

Regulatory Information

Company Information

Active Ingredients

CROSCARMELLOSE SODIUM

LACTOSE MONOHYDRATE

MAGNESIUM STEARATE

STARCH, CORN

POVIDONE K30

Active Moieties

ALLOPURINOL