Product NDC: | 68788-9957 |
Proprietary Name: | cephalexin |
Non Proprietary Name: | Cephalexin |
Active Ingredient(s): | 250 mg/5mL & nbsp; Cephalexin |
Administration Route(s): | ORAL |
Dosage Form(s): | FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-9957 |
Labeler Name: | Preferred Pharmaceuticals, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065234 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120110 |
Package NDC: | 68788-9957-2 |
Package Description: | 200 mL in 1 BOTTLE (68788-9957-2) |
NDC Code | 68788-9957-2 |
Proprietary Name | cephalexin |
Package Description | 200 mL in 1 BOTTLE (68788-9957-2) |
Product NDC | 68788-9957 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Cephalexin |
Dosage Form Name | FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20120110 |
Marketing Category Name | ANDA |
Labeler Name | Preferred Pharmaceuticals, Inc |
Substance Name | CEPHALEXIN |
Strength Number | 250 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |