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Glimepiride - 43063-122-90 - (Glimepiride)

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Drug Information of Glimepiride

Product NDC: 43063-122
Proprietary Name: Glimepiride
Non Proprietary Name: Glimepiride
Active Ingredient(s): 4    mg/1 & nbsp;   Glimepiride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glimepiride

Product NDC: 43063-122
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077091
Marketing Category: ANDA
Start Marketing Date: 20051006

Package Information of Glimepiride

Package NDC: 43063-122-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (43063-122-90)

NDC Information of Glimepiride

NDC Code 43063-122-90
Proprietary Name Glimepiride
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (43063-122-90)
Product NDC 43063-122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glimepiride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20051006
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name GLIMEPIRIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glimepiride


General Information