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cephalexin
cephalexin - 50436-0117-4 - (cephalexin)
Drug Information of cephalexin
| Product NDC: | 50436-0117 |
| Proprietary Name: | cephalexin |
| Non Proprietary Name: | cephalexin |
| Active Ingredient(s): | 500 mg/1 & nbsp; cephalexin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of cephalexin
| Product NDC: | 50436-0117 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062791 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100621 |
Package Information of cephalexin
| Package NDC: | 50436-0117-4 |
| Package Description: | 14 CAPSULE in 1 BOTTLE (50436-0117-4) |
NDC Information of cephalexin
| NDC Code | 50436-0117-4 |
| Proprietary Name | cephalexin |
| Package Description | 14 CAPSULE in 1 BOTTLE (50436-0117-4) |
| Product NDC | 50436-0117 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cephalexin |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100621 |
| Marketing Category Name | ANDA |
| Labeler Name | Unit Dose Services |
| Substance Name | CEPHALEXIN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
