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Cephalexin
Cephalexin - 21695-789-20 - (Cephalexin)
Drug Information of Cephalexin
| Product NDC: | 21695-789 |
| 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: | 21695-789 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062703 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100921 |
Package Information of Cephalexin
| Package NDC: | 21695-789-20 |
| Package Description: | 200 mL in 1 BOTTLE (21695-789-20) |
NDC Information of Cephalexin
| NDC Code | 21695-789-20 |
| Proprietary Name | Cephalexin |
| Package Description | 200 mL in 1 BOTTLE (21695-789-20) |
| Product NDC | 21695-789 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cephalexin |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20100921 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | CEPHALEXIN |
| Strength Number | 125 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
