AMARYL - 0039-0222-10 - (glimepiride)

Alphabetical Index


Drug Information of AMARYL

Product NDC: 0039-0222
Proprietary Name: AMARYL
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 AMARYL

Product NDC: 0039-0222
Labeler Name: Sanofi-Aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020496
Marketing Category: NDA
Start Marketing Date: 20090618

Package Information of AMARYL

Package NDC: 0039-0222-10
Package Description: 100 TABLET in 1 BOTTLE (0039-0222-10)

NDC Information of AMARYL

NDC Code 0039-0222-10
Proprietary Name AMARYL
Package Description 100 TABLET in 1 BOTTLE (0039-0222-10)
Product NDC 0039-0222
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name glimepiride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090618
Marketing Category Name NDA
Labeler Name Sanofi-Aventis U.S. LLC
Substance Name GLIMEPIRIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of AMARYL


General Information