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cephalexin
cephalexin - 68788-9957-1 - (Cephalexin)
Drug Information of cephalexin
| 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) |
Labeler Information of cephalexin
| 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 Information of cephalexin
| Package NDC: | 68788-9957-1 |
| Package Description: | 100 mL in 1 BOTTLE (68788-9957-1) |
NDC Information of cephalexin
| NDC Code | 68788-9957-1 |
| Proprietary Name | cephalexin |
| Package Description | 100 mL in 1 BOTTLE (68788-9957-1) |
| 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] |
