Keflex - 59630-115-05 - (cephalexin)

Alphabetical Index


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]

Complete Information of Keflex


General Information