Product NDC: | 0781-6203 |
Proprietary Name: | Cefprozil |
Non Proprietary Name: | Cefprozil |
Active Ingredient(s): | 250 mg/5mL & nbsp; Cefprozil |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0781-6203 |
Labeler Name: | Sandoz Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065257 |
Marketing Category: | ANDA |
Start Marketing Date: | 20051205 |
Package NDC: | 0781-6203-46 |
Package Description: | 100 mL in 1 BOTTLE (0781-6203-46) |
NDC Code | 0781-6203-46 |
Proprietary Name | Cefprozil |
Package Description | 100 mL in 1 BOTTLE (0781-6203-46) |
Product NDC | 0781-6203 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Cefprozil |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20051205 |
Marketing Category Name | ANDA |
Labeler Name | Sandoz Inc |
Substance Name | CEFPROZIL |
Strength Number | 250 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |