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cephalexin
cephalexin - 42043-142-38 - (cephalexin)
Drug Information of cephalexin
| Product NDC: | 42043-142 |
| Proprietary Name: | cephalexin |
| Non Proprietary Name: | cephalexin |
| Active Ingredient(s): | 125 mg/5mL & nbsp; cephalexin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of cephalexin
| Product NDC: | 42043-142 |
| Labeler Name: | Karalex Pharma LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065326 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070712 |
Package Information of cephalexin
| Package NDC: | 42043-142-38 |
| Package Description: | 100 mL in 1 BOTTLE (42043-142-38) |
NDC Information of cephalexin
| NDC Code | 42043-142-38 |
| Proprietary Name | cephalexin |
| Package Description | 100 mL in 1 BOTTLE (42043-142-38) |
| Product NDC | 42043-142 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cephalexin |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20070712 |
| Marketing Category Name | ANDA |
| Labeler Name | Karalex Pharma LLC |
| Substance Name | CEPHALEXIN |
| Strength Number | 125 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
