Allopurinol

Product NDC
63304-539
11-digit product format
633040539
Labeler code
63304
Product ID
63304-539_205867ab-d40a-4f09-8338-4509e576ac95
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Allopurinol
Dosage form
TABLET
Route
ORAL
Labeler
Ranbaxy Pharmaceuticals Inc.
Application
ANDA090637
Marketing category
ANDA
Marketing start
2011-06-06
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
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ee55bab-4ea8-ac26-c688-380cfbcd5c03Product name720260127
de89a493-168f-43fa-9852-1f15e00dbb17Product name120221110
4a2a34d6-1853-423b-9e0c-360370b95802Product name120171006

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63304-539-01EA - Each63304-5395e4fc039-c27c-44cf-a4f9-96845ec3bf6312012-07-24
63304-539-10EA - Each63304-539a22c0558-70c7-4a4e-9aa5-18b97ff3d56612012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALLOPURINOLACTIVE INGREDIENT63CZ7GJN5IALLOPURINOL TABLET [BLENHEIM PHARMACAL, INC.]3
ALLOPURINOLACTIVE MOIETY63CZ7GJN5IALLOPURINOL TABLET [BLENHEIM PHARMACAL, INC.]3
FD&C YELLOW NO. 6INACTIVE INGREDIENTH77VEI93A8ALLOPURINOL TABLET [BLENHEIM PHARMACAL, INC.]3
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XALLOPURINOL TABLET [BLENHEIM PHARMACAL, INC.]3
POVIDONEINACTIVE INGREDIENTFZ989GH94EALLOPURINOL TABLET [BLENHEIM PHARMACAL, INC.]3
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2ALLOPURINOL TABLET [BLENHEIM PHARMACAL, INC.]3
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJALLOPURINOL TABLET [BLENHEIM PHARMACAL, INC.]3
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APALLOPURINOL TABLET [BLENHEIM PHARMACAL, INC.]3
ALLOPURINOLACTIVE INGREDIENT63CZ7GJN5IALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]2
ALLOPURINOLACTIVE MOIETY63CZ7GJN5IALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]2
FD&C YELLOW NO. 6INACTIVE INGREDIENTH77VEI93A8ALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]2
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]2
POVIDONEINACTIVE INGREDIENTFZ989GH94EALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]2
POVIDONESINACTIVE INGREDIENTFZ989GH94EALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]2
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2ALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]2
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APALLOPURINOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197319allopurinol 100 MG Oral TabletPSN4aaacdca-60d6-4757-a1b1-3bee82b035f83
197320allopurinol 300 MG Oral TabletPSN4aaacdca-60d6-4757-a1b1-3bee82b035f83
197319allopurinol 100 MG Oral TabletSCD4aaacdca-60d6-4757-a1b1-3bee82b035f83
197320allopurinol 300 MG Oral TabletSCD4aaacdca-60d6-4757-a1b1-3bee82b035f83
197319allopurinol 100 MG Oral TabletPSNb9e592ce-942f-4943-a802-bca1c679999f2
197320allopurinol 300 MG Oral TabletPSNb9e592ce-942f-4943-a802-bca1c679999f2
197319allopurinol 100 MG Oral TabletSCDb9e592ce-942f-4943-a802-bca1c679999f2
197320allopurinol 300 MG Oral TabletSCDb9e592ce-942f-4943-a802-bca1c679999f2