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Chlorpropamide
Chlorpropamide - 55289-066-90 - (chlorpropamide)
Drug Information of Chlorpropamide
| Product NDC: | 55289-066 |
| Proprietary Name: | Chlorpropamide |
| Non Proprietary Name: | chlorpropamide |
| Active Ingredient(s): | 250 mg/1 & nbsp; chlorpropamide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chlorpropamide
| Product NDC: | 55289-066 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088549 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110504 |
Package Information of Chlorpropamide
| Package NDC: | 55289-066-90 |
| Package Description: | 90 TABLET in 1 BOTTLE, PLASTIC (55289-066-90) |
NDC Information of Chlorpropamide
| NDC Code | 55289-066-90 |
| Proprietary Name | Chlorpropamide |
| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (55289-066-90) |
| Product NDC | 55289-066 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | chlorpropamide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110504 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | CHLORPROPAMIDE |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |
