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Glyburide
Glyburide - 59762-7022-9 - (Glyburide)
Drug Information of Glyburide
| Product NDC: | 59762-7022 |
| Proprietary Name: | Glyburide |
| Non Proprietary Name: | Glyburide |
| Active Ingredient(s): | 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: | 59762-7022 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077537 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071018 |
Package Information of Glyburide
| Package NDC: | 59762-7022-9 |
| Package Description: | 100 TABLET in 1 BOTTLE (59762-7022-9) |
NDC Information of Glyburide
| NDC Code | 59762-7022-9 |
| Proprietary Name | Glyburide |
| Package Description | 100 TABLET in 1 BOTTLE (59762-7022-9) |
| Product NDC | 59762-7022 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Glyburide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20071018 |
| Marketing Category Name | ANDA |
| Labeler Name | Greenstone LLC |
| Substance Name | GLYBURIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |
