Glipizide

Product NDC
61919-286
11-digit product format
619190286
Labeler code
61919
Product ID
61919-286_9c9437d9-bfdd-2a03-e053-2a95a90aeded
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glipizide
Dosage form
TABLET
Route
ORAL
Labeler
DIRECT RX
Application
ANDA077820
Marketing category
ANDA
Marketing start
2014-01-01
Marketing end
0000-00-00
Substance
GLIPIZIDE
Active strength
5 mg/1
Pharmacologic classes
Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61919-286-602022-01-28C16284748780-1d6a99b39-6c92-a426-e053-dadaa90af4c2Glipizide
61919-286-302020-01-31C16284748780-19d75b9cf-d286-f424-e053-dadaa90a57ceGLIPIZIDE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61919-286-30Glipizide30 in 1 BOTTLETABLET308
61919-286-90Glipizide90 in 1 BOTTLETABLET908
61919-286-60Glipizide60 in 1 BOTTLETABLET604

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
61919-286-90EA - Each61919-28651e3bc29-9428-4de7-8c08-bfa233b17f4d12014-12-01

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GlipizideACTIVE INGREDIENTX7WDT95N5CGLIPIZIDE TABLET [DIRECT RX]1
GLIPIZIDEACTIVE MOIETYX7WDT95N5CGLIPIZIDE TABLET [DIRECT RX]1
cellulose, microcrystallineINACTIVE INGREDIENTOP1R32D61UGLIPIZIDE TABLET [DIRECT RX]1
lactose monohydrateINACTIVE INGREDIENTEWQ57Q8I5XGLIPIZIDE TABLET [DIRECT RX]1
silicon dioxideINACTIVE INGREDIENTETJ7Z6XBU4GLIPIZIDE TABLET [DIRECT RX]1
starch, cornINACTIVE INGREDIENTO8232NY3SJGLIPIZIDE TABLET [DIRECT RX]1
starch, potatoINACTIVE INGREDIENT8I089SAH3TGLIPIZIDE TABLET [DIRECT RX]1
stearic acidINACTIVE INGREDIENT4ELV7Z65APGLIPIZIDE TABLET [DIRECT RX]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61919-286GLIPIZIDE TABLET [DIRECT RX]8Legacy NDC, 2 package rows20170224_dddf88bd-fdc9-4794-859f-8a54bf6e385a.zip
61919-286GLIPIZIDE TABLET [DIRECT RX]4Legacy NDC, 1 package rows20200121_17bdb2e2-9b1d-4376-a707-47f0710755f0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310490glipiZIDE 5 MG Oral TabletPSNdddf88bd-fdc9-4794-859f-8a54bf6e385a8
310490glipizide 5 MG Oral TabletSCDdddf88bd-fdc9-4794-859f-8a54bf6e385a8
310490glipiZIDE 5 MG Oral TabletPSN17bdb2e2-9b1d-4376-a707-47f0710755f04
310490glipizide 5 MG Oral TabletSCD17bdb2e2-9b1d-4376-a707-47f0710755f04

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61919-286-306191902863030 in 1 BOTTLEHistorical
61919-286-606191902866060 TABLET in 1 BOTTLE (61919-286-60) 60 tablet2017-02-240000-00-00NoNoCurrent
61919-286-906191902869090 in 1 BOTTLEHistorical