Glimepiride

Product NDC
50090-1526
11-digit product format
500901526
Labeler code
50090
Product ID
50090-1526_db1f3e91-4e62-4447-9e37-52f515e0818e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Glimepiride
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078181
Marketing category
ANDA
Marketing start
2007-08-23
Marketing end
0000-00-00
Substance
GLIMEPIRIDE
Active strength
2 mg/1
Pharmacologic classes
Sulfonylurea [EPC],Sulfonylurea Compounds [CS]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-1526-0EA - Each50090-1526c5e5827d-6b0c-4a3b-89cb-515a244533b312018-11-06
50090-1526-1EA - Each50090-1526ce5f34e5-cf9c-41cc-b2ec-b841d23f564f12018-08-13
50090-1526-3EA - Each50090-1526cc468eb4-ed32-4ceb-8fff-9e709ba60f3112018-08-13
50090-1526-4EA - Each50090-1526894cf7fb-9104-454f-ab24-e1f6e4ab95b512021-09-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-1526GLIMEPIRIDE TABLET [A-S MEDICATION SOLUTIONS]18Legacy NDC20230623_dac7b655-d2e3-458a-9a8d-677757ba2a75.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-1526-05009015260030 TABLET in 1 BOTTLE (50090-1526-0) 30 tablet2014-12-110000-00-00NoNoCurrent
50090-1526-150090152601100 TABLET in 1 BOTTLE (50090-1526-1) 100 tablet2014-12-110000-00-00NoNoCurrent
50090-1526-35009015260390 TABLET in 1 BOTTLE (50090-1526-3) 90 tablet2014-12-110000-00-00NoNoCurrent
50090-1526-450090152604180 TABLET in 1 BOTTLE (50090-1526-4) 180 tablet2019-01-260000-00-00NoNoCurrent