Product NDC: | 54868-5243 |
Proprietary Name: | Glyburide and Metformin |
Non Proprietary Name: | Glyburide and Metformin |
Active Ingredient(s): | 5; 500 mg/1; mg/1 & nbsp; Glyburide and Metformin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5243 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076345 |
Marketing Category: | ANDA |
Start Marketing Date: | 20050307 |
Package NDC: | 54868-5243-4 |
Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (54868-5243-4) |
NDC Code | 54868-5243-4 |
Proprietary Name | Glyburide and Metformin |
Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (54868-5243-4) |
Product NDC | 54868-5243 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Glyburide and Metformin |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20050307 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | GLYBURIDE; METFORMIN HYDROCHLORIDE |
Strength Number | 5; 500 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient],Biguanide [EPC],Biguanides [Chemical/Ingredient] |