Glipizide

Product NDC
68788-0141
11-digit product format
687880141
Labeler code
68788
Product ID
68788-0141_68908298-c541-479c-bc63-14c78371946b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glipizide
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA075795
Marketing category
ANDA
Marketing start
2013-02-18
Substance
GLIPIZIDE
Active strength
5 mg/1
Pharmacologic classes
Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Glipizide
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GLIPIZIDE5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiX7WDT95N5C
Rxcui310488, 310490

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ec4adfb0-aabc-95b9-ad07-5cb8f8533a09Product name220250625
b1de1ca9-d9db-4f4b-2103-09e2014d30d5Product name520180912
2dee091b-3b8c-d27a-b1ba-fcb0d32e776aProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68788-0141-1Glipizide100 in 1 BOTTLETABLET10014
68788-0141-3Glipizide30 in 1 BOTTLETABLET3014
68788-0141-6Glipizide60 in 1 BOTTLETABLET6014
68788-0141-9Glipizide90 in 1 BOTTLETABLET9014

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GLIPIZIDEACTIVE INGREDIENTX7WDT95N5CGLIPIZIDE TABLET [PREFERRED PHARMACEUTICALS, INC.]3
GLIPIZIDEACTIVE MOIETYX7WDT95N5CGLIPIZIDE TABLET [PREFERRED PHARMACEUTICALS, INC.]3
ANHYDROUS LACTOSEINACTIVE INGREDIENT3SY5LH9PMKGLIPIZIDE TABLET [PREFERRED PHARMACEUTICALS, INC.]3
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30GLIPIZIDE TABLET [PREFERRED PHARMACEUTICALS, INC.]3
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4GLIPIZIDE TABLET [PREFERRED PHARMACEUTICALS, INC.]3
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2GLIPIZIDE TABLET [PREFERRED PHARMACEUTICALS, INC.]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68788-0141GLIPIZIDE TABLET [PREFERRED PHARMACEUTICALS, INC.]12Current NDC, Legacy NDC, 4 package rows20240514_097424ef-612f-4bc2-809a-e5bb8eeae244.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310488glipiZIDE 10 MG Oral TabletPSN097424ef-612f-4bc2-809a-e5bb8eeae24414
310490glipiZIDE 5 MG Oral TabletPSN097424ef-612f-4bc2-809a-e5bb8eeae24414
310488glipizide 10 MG Oral TabletSCD097424ef-612f-4bc2-809a-e5bb8eeae24414
310490glipizide 5 MG Oral TabletSCD097424ef-612f-4bc2-809a-e5bb8eeae24414

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-0141-168788014101100 TABLET in 1 BOTTLE (68788-0141-1) 100 tablet2013-02-180000-00-00NoNoCurrent
68788-0141-36878801410330 TABLET in 1 BOTTLE (68788-0141-3) 30 tablet2013-02-180000-00-00NoNoCurrent
68788-0141-66878801410660 TABLET in 1 BOTTLE (68788-0141-6) 60 tablet2013-02-180000-00-00NoNoCurrent
68788-0141-96878801410990 TABLET in 1 BOTTLE (68788-0141-9) 90 tablet2013-02-180000-00-00NoNoCurrent