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Keflex
Keflex - 59630-115-05 - (cephalexin)
Drug Information of Keflex
| Product NDC: | 59630-115 |
| Proprietary Name: | Keflex |
| Non Proprietary Name: | cephalexin |
| Active Ingredient(s): | 750 mg/1 & nbsp; cephalexin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Keflex
| Product NDC: | 59630-115 |
| Labeler Name: | Shionogi Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050405 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110729 |
Package Information of Keflex
| Package NDC: | 59630-115-05 |
| Package Description: | 50 CAPSULE in 1 BOTTLE (59630-115-05) |
NDC Information of Keflex
| NDC Code | 59630-115-05 |
| Proprietary Name | Keflex |
| Package Description | 50 CAPSULE in 1 BOTTLE (59630-115-05) |
| Product NDC | 59630-115 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cephalexin |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110729 |
| Marketing Category Name | NDA |
| Labeler Name | Shionogi Inc. |
| Substance Name | CEPHALEXIN |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
