Glipizide

Product NDC
69584-310
11-digit product format
695840310
Labeler code
69584
Product ID
69584-310_496b39ed-3ca0-4265-a401-674fe6d4a0d1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glipizide
Dosage form
TABLET
Route
ORAL
Labeler
Oxford Pharmaceuticals, LLC
Application
ANDA074378
Marketing category
ANDA
Marketing start
2025-05-01
Substance
GLIPIZIDE
Active strength
10 mg/1
Pharmacologic classes
Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Glipizide
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GLIPIZIDE10 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
69584-310-10Glipizide100 in 1 BOTTLETABLET1002
69584-310-50Glipizide500 in 1 BOTTLETABLET5002
69584-310-90Glipizide1000 in 1 BOTTLETABLET10002

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69584-310-10EA - Each69584-310ef598412-ca80-4849-aaf7-25e400d92d1812025-05-14
69584-310-50EA - Each69584-3101079b24c-73c5-447d-80d9-eb3706f5d61a12025-05-14
69584-310-90EA - Each69584-310359f4914-9631-4fc2-9a00-cedc3993f97412025-05-14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69584-310GLIPIZIDE TABLET [OXFORD PHARMACEUTICALS, LLC]2Current NDC, 3 package rows20250502_87cd4930-ba68-4acf-bf74-619c477b557d.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310488glipiZIDE 10 MG Oral TabletPSN87cd4930-ba68-4acf-bf74-619c477b557d2
310490glipiZIDE 5 MG Oral TabletPSN87cd4930-ba68-4acf-bf74-619c477b557d2
310488glipizide 10 MG Oral TabletSCD87cd4930-ba68-4acf-bf74-619c477b557d2
310490glipizide 5 MG Oral TabletSCD87cd4930-ba68-4acf-bf74-619c477b557d2
310488glipiZIDE 10 MG Oral TabletPSN410bf280-838d-45af-9b60-15f94ded75811
310488glipiZIDE 10 MG Oral TabletPSNf5d7a98c-d1d4-43b9-8d7e-830a33ae0c241
310490glipiZIDE 5 MG Oral TabletPSNf5d7a98c-d1d4-43b9-8d7e-830a33ae0c241
310488glipizide 10 MG Oral TabletSCD410bf280-838d-45af-9b60-15f94ded75811
310488glipizide 10 MG Oral TabletSCDf5d7a98c-d1d4-43b9-8d7e-830a33ae0c241
310490glipizide 5 MG Oral TabletSCDf5d7a98c-d1d4-43b9-8d7e-830a33ae0c241

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69584-310-1069584031010100 TABLET in 1 BOTTLE (69584-310-10) 100 tablet2025-05-01NoNoHistorical
69584-310-5069584031050500 TABLET in 1 BOTTLE (69584-310-50) 500 tablet2025-05-01NoNoHistorical
69584-310-90695840310901000 TABLET in 1 BOTTLE (69584-310-90) 1000 tablet2025-05-01NoNoHistorical