Glyburide

Product NDC
66336-712
11-digit product format
663360712
Labeler code
66336
Product ID
66336-712_57076caf-0ccd-484f-9e80-8bd934593387
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glyburide
Dosage form
TABLET
Route
ORAL
Labeler
Dispensing Solutions, Inc.
Application
ANDA074686
Marketing category
ANDA
Marketing start
1999-05-12
Marketing end
0000-00-00
Substance
GLYBURIDE
Active strength
6 mg/1
Pharmacologic classes
Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
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
bea938a6-c880-985b-d27b-b59b0d8b5a77Product name320170626
0600b0d3-c32a-40bb-8d87-3a2934cd8f2fProduct name120170616
64b2b6e2-1c04-cf4a-db4c-078ed10e1dd6Product name220160609
5a2baaae-1290-c05e-207f-b1367e9eb46aProduct name220151005
b044018d-bcdc-e68d-63da-1ad6886aea64Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66336-712-902019-11-27C16284748780-19855d018-dded-cd31-e053-dbdaa90ab51aGLYBURIDE TABLETS (MICRONIZED), USP Rx only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66336-712-90Glyburide90 in 1 BOTTLETABLET901

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66336-712-90EA - Each66336-71214991db6-6813-46d9-bee9-c2810df2657212013-07-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GLYBURIDEACTIVE INGREDIENTSX6K58TVWCGLYBURIDE TABLET [DISPENSING SOLUTIONS, INC.]1
GLYBURIDEACTIVE MOIETYSX6K58TVWCGLYBURIDE TABLET [DISPENSING SOLUTIONS, INC.]1
ALUMINUM OXIDEINACTIVE INGREDIENTLMI26O6933GLYBURIDE TABLET [DISPENSING SOLUTIONS, INC.]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UGLYBURIDE TABLET [DISPENSING SOLUTIONS, INC.]1
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBDGLYBURIDE TABLET [DISPENSING SOLUTIONS, INC.]1
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKGLYBURIDE TABLET [DISPENSING SOLUTIONS, INC.]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30GLYBURIDE TABLET [DISPENSING SOLUTIONS, INC.]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4GLYBURIDE TABLET [DISPENSING SOLUTIONS, INC.]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2GLYBURIDE TABLET [DISPENSING SOLUTIONS, INC.]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJGLYBURIDE TABLET [DISPENSING SOLUTIONS, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66336-712GLYBURIDE TABLET [DISPENSING SOLUTIONS, INC.]1Legacy NDC, 1 package rows20130618_ad8c8c38-73d3-41c1-94d5-f7cf9e98e8e9.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310539glyBURIDE 6 MG Oral TabletPSNad8c8c38-73d3-41c1-94d5-f7cf9e98e8e91
310539glyburide 6 MG Oral TabletSCDad8c8c38-73d3-41c1-94d5-f7cf9e98e8e91

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
66336-712-906633607129090 in 1 BOTTLEHistorical