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Tolbutamide
Tolbutamide - 0378-0215-01 - (tolbutamide)
Drug Information of Tolbutamide
| Product NDC: | 0378-0215 |
| Proprietary Name: | Tolbutamide |
| Non Proprietary Name: | tolbutamide |
| Active Ingredient(s): | 500 mg/1 & nbsp; tolbutamide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tolbutamide
| Product NDC: | 0378-0215 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA086445 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130506 |
Package Information of Tolbutamide
| Package NDC: | 0378-0215-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0215-01) |
NDC Information of Tolbutamide
| NDC Code | 0378-0215-01 |
| Proprietary Name | Tolbutamide |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0378-0215-01) |
| Product NDC | 0378-0215 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tolbutamide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130506 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | TOLBUTAMIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |
