Allopurinol

Product NDC
67544-988
11-digit product format
675440988
Labeler code
67544
Product ID
67544-988_64ebbee6-7e2a-455f-9f96-92bc25d3e691
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
allopurinol
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, Inc.
Application
ANDA075798
Marketing category
ANDA
Marketing start
2003-06-27
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
2017-12-31
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 Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67544-988-30Allopurinol30 in 1 BOTTLE, PLASTICTABLET302
67544-988-60Allopurinol90 in 1 BOTTLE, PLASTICTABLET902
67544-988-80Allopurinol180 in 1 BOTTLE, PLASTICTABLET1802

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67544-988-30EA - Each67544-9880ff50768-5e1b-47d7-9a2a-fc52252aeedb12013-02-13
67544-988-60EA - Each67544-988848fa8b7-6e19-43cc-b8b8-ac27d69ec74612012-07-24
67544-988-80EA - Each67544-988adc2632b-3d32-4c67-b0f6-ba0fa90f5f4112012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALLOPURINOLACTIVE INGREDIENT63CZ7GJN5IALLOPURINOL TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, INC.]2
ALLOPURINOLACTIVE MOIETY63CZ7GJN5IALLOPURINOL TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, INC.]2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UALLOPURINOL TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, INC.]2
FD&C YELLOW NO. 6INACTIVE INGREDIENTH77VEI93A8ALLOPURINOL TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, INC.]2
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XALLOPURINOL TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, INC.]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30ALLOPURINOL TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, INC.]2
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4ALLOPURINOL TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, INC.]2
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2ALLOPURINOL TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, INC.]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67544-988ALLOPURINOL TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, INC.]2Legacy NDC, 3 package rows20120327_548f6fbb-155f-45ff-ab44-0a70adad4424.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197319allopurinol 100 MG Oral TabletPSN548f6fbb-155f-45ff-ab44-0a70adad44242
197320allopurinol 300 MG Oral TabletPSN548f6fbb-155f-45ff-ab44-0a70adad44242
197319allopurinol 100 MG Oral TabletSCD548f6fbb-155f-45ff-ab44-0a70adad44242
197320allopurinol 300 MG Oral TabletSCD548f6fbb-155f-45ff-ab44-0a70adad44242

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
67544-988-306754409883030 in 1 BOTTLE, PLASTICHistorical
67544-988-606754409886090 in 1 BOTTLE, PLASTICHistorical
67544-988-8067544098880180 in 1 BOTTLE, PLASTICHistorical