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Glyburide (micronized) and Metformin Hydrochloride
Glyburide (micronized) and Metformin Hydrochloride - 45963-753-04 - (Glyburide (micronized) and Metformin Hydrochloride)
Drug Information of Glyburide (micronized) and Metformin Hydrochloride
| Product NDC: | 45963-753 |
| Proprietary Name: | Glyburide (micronized) and Metformin Hydrochloride |
| Non Proprietary Name: | Glyburide (micronized) and Metformin Hydrochloride |
| Active Ingredient(s): | 5; 500 mg/1; mg/1 & nbsp; Glyburide (micronized) and Metformin Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Glyburide (micronized) and Metformin Hydrochloride
| Product NDC: | 45963-753 |
| Labeler Name: | Actavis Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076716 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110622 |
Package Information of Glyburide (micronized) and Metformin Hydrochloride
| Package NDC: | 45963-753-04 |
| Package Description: | 500 TABLET in 1 BOTTLE (45963-753-04) |
NDC Information of Glyburide (micronized) and Metformin Hydrochloride
| NDC Code | 45963-753-04 |
| Proprietary Name | Glyburide (micronized) and Metformin Hydrochloride |
| Package Description | 500 TABLET in 1 BOTTLE (45963-753-04) |
| Product NDC | 45963-753 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Glyburide (micronized) and Metformin Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110622 |
| Marketing Category Name | ANDA |
| Labeler Name | Actavis 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] |
