Cephalexin - 52959-031-20 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 52959-031
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: 52959-031
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065215
Marketing Category: ANDA
Start Marketing Date: 20060201

Package Information of Cephalexin

Package NDC: 52959-031-20
Package Description: 20 CAPSULE in 1 BOTTLE, PLASTIC (52959-031-20)

NDC Information of Cephalexin

NDC Code 52959-031-20
Proprietary Name Cephalexin
Package Description 20 CAPSULE in 1 BOTTLE, PLASTIC (52959-031-20)
Product NDC 52959-031
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20060201
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, 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