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GLYBURIDE AND METFORMIN HYDROCHLORIDE
GLYBURIDE AND METFORMIN HYDROCHLORIDE - 55111-696-10 - (GLYBURIDE AND METFORMIN HYDROCHLORIDE)
Drug Information of GLYBURIDE AND METFORMIN HYDROCHLORIDE
| Product NDC: | 55111-696 |
| Proprietary Name: | GLYBURIDE AND METFORMIN HYDROCHLORIDE |
| Non Proprietary Name: | GLYBURIDE AND METFORMIN HYDROCHLORIDE |
| Active Ingredient(s): | 2.5; 500 mg/1; mg/1 & nbsp; GLYBURIDE AND METFORMIN HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GLYBURIDE AND METFORMIN HYDROCHLORIDE
| Product NDC: | 55111-696 |
| Labeler Name: | Dr. Reddy's Laboratories Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079009 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090630 |
Package Information of GLYBURIDE AND METFORMIN HYDROCHLORIDE
| Package NDC: | 55111-696-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE (55111-696-10) |
NDC Information of GLYBURIDE AND METFORMIN HYDROCHLORIDE
| NDC Code | 55111-696-10 |
| Proprietary Name | GLYBURIDE AND METFORMIN HYDROCHLORIDE |
| Package Description | 1000 TABLET in 1 BOTTLE (55111-696-10) |
| Product NDC | 55111-696 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | GLYBURIDE AND METFORMIN HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090630 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr. Reddy's Laboratories Limited |
| Substance Name | GLYBURIDE; METFORMIN HYDROCHLORIDE |
| Strength Number | 2.5; 500 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient],Biguanide [EPC],Biguanides [Chemical/Ingredient] |
