Product NDC: | 68180-401 |
Proprietary Name: | CEFPROZIL |
Non Proprietary Name: | CEFPROZIL |
Active Ingredient(s): | 125 mg/5mL & nbsp; CEFPROZIL |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68180-401 |
Labeler Name: | LUPIN PHARMACEUTICALS INC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065261 |
Marketing Category: | ANDA |
Start Marketing Date: | 20051201 |
Package NDC: | 68180-401-01 |
Package Description: | 50 mL in 1 BOTTLE (68180-401-01) |
NDC Code | 68180-401-01 |
Proprietary Name | CEFPROZIL |
Package Description | 50 mL in 1 BOTTLE (68180-401-01) |
Product NDC | 68180-401 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CEFPROZIL |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20051201 |
Marketing Category Name | ANDA |
Labeler Name | LUPIN PHARMACEUTICALS INC |
Substance Name | CEFPROZIL |
Strength Number | 125 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |