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DiaBeta
DiaBeta - 0039-0051-50 - (glyburide)
Drug Information of DiaBeta
| Product NDC: | 0039-0051 |
| Proprietary Name: | DiaBeta |
| Non Proprietary Name: | glyburide |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; glyburide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DiaBeta
| Product NDC: | 0039-0051 |
| Labeler Name: | Sanofi-Aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017532 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090601 |
Package Information of DiaBeta
| Package NDC: | 0039-0051-50 |
| Package Description: | 500 TABLET in 1 BOTTLE (0039-0051-50) |
NDC Information of DiaBeta
| NDC Code | 0039-0051-50 |
| Proprietary Name | DiaBeta |
| Package Description | 500 TABLET in 1 BOTTLE (0039-0051-50) |
| Product NDC | 0039-0051 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | glyburide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090601 |
| Marketing Category Name | NDA |
| Labeler Name | Sanofi-Aventis U.S. LLC |
| Substance Name | GLYBURIDE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |
