Product NDC: | 0378-0197 |
Proprietary Name: | Chlorpropamide |
Non Proprietary Name: | chlorpropamide |
Active Ingredient(s): | 100 mg/1 & nbsp; chlorpropamide |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0378-0197 |
Labeler Name: | Mylan Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA088549 |
Marketing Category: | ANDA |
Start Marketing Date: | 19840601 |
Package NDC: | 0378-0197-05 |
Package Description: | 500 TABLET in 1 BOTTLE, PLASTIC (0378-0197-05) |
NDC Code | 0378-0197-05 |
Proprietary Name | Chlorpropamide |
Package Description | 500 TABLET in 1 BOTTLE, PLASTIC (0378-0197-05) |
Product NDC | 0378-0197 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | chlorpropamide |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19840601 |
Marketing Category Name | ANDA |
Labeler Name | Mylan Pharmaceuticals Inc. |
Substance Name | CHLORPROPAMIDE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |