Cephalexin - 10544-082-28 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 10544-082
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: 10544-082
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062713
Marketing Category: ANDA
Start Marketing Date: 20120801

Package Information of Cephalexin

Package NDC: 10544-082-28
Package Description: 28 CAPSULE in 1 BOTTLE (10544-082-28)

NDC Information of Cephalexin

NDC Code 10544-082-28
Proprietary Name Cephalexin
Package Description 28 CAPSULE in 1 BOTTLE (10544-082-28)
Product NDC 10544-082
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120801
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, Inc.
Substance Name CEPHALEXIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cephalexin


General Information