Cephalexin - 67877-254-01 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 67877-254
Proprietary Name: Cephalexin
Non Proprietary Name: Cephalexin
Active Ingredient(s): 333    mg/1 & nbsp;   Cephalexin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Cephalexin

Product NDC: 67877-254
Labeler Name: Ascend Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090836
Marketing Category: ANDA
Start Marketing Date: 20120604

Package Information of Cephalexin

Package NDC: 67877-254-01
Package Description: 100 CAPSULE in 1 BOTTLE (67877-254-01)

NDC Information of Cephalexin

NDC Code 67877-254-01
Proprietary Name Cephalexin
Package Description 100 CAPSULE in 1 BOTTLE (67877-254-01)
Product NDC 67877-254
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120604
Marketing Category Name ANDA
Labeler Name Ascend Laboratories, LLC
Substance Name CEPHALEXIN
Strength Number 333
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cephalexin


General Information