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Glyburide
Glyburide - 0093-9433-01 - (glyburide)
Drug Information of Glyburide
| Product NDC: | 0093-9433 |
| Proprietary Name: | Glyburide |
| 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 Glyburide
| Product NDC: | 0093-9433 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017532 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19940401 |
Package Information of Glyburide
| Package NDC: | 0093-9433-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0093-9433-01) |
NDC Information of Glyburide
| NDC Code | 0093-9433-01 |
| Proprietary Name | Glyburide |
| Package Description | 100 TABLET in 1 BOTTLE (0093-9433-01) |
| Product NDC | 0093-9433 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | glyburide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19940401 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | GLYBURIDE |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |
