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Glimepiride - 68084-326-01 - (Glimepiride)

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Drug Information of Glimepiride

Product NDC: 68084-326
Proprietary Name: Glimepiride
Non Proprietary Name: Glimepiride
Active Ingredient(s): 2    mg/1 & nbsp;   Glimepiride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glimepiride

Product NDC: 68084-326
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077091
Marketing Category: ANDA
Start Marketing Date: 20090512

Package Information of Glimepiride

Package NDC: 68084-326-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-326-01) > 10 TABLET in 1 BLISTER PACK (68084-326-11)

NDC Information of Glimepiride

NDC Code 68084-326-01
Proprietary Name Glimepiride
Package Description 10 BLISTER PACK in 1 CARTON (68084-326-01) > 10 TABLET in 1 BLISTER PACK (68084-326-11)
Product NDC 68084-326
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glimepiride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090512
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name GLIMEPIRIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glimepiride


General Information