Cephalexin - 52959-030-40 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 52959-030
Proprietary Name: Cephalexin
Non Proprietary Name: Cephalexin
Active Ingredient(s): 250    mg/1 & nbsp;   Cephalexin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Cephalexin

Product NDC: 52959-030
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065229
Marketing Category: ANDA
Start Marketing Date: 20051201

Package Information of Cephalexin

Package NDC: 52959-030-40
Package Description: 40 CAPSULE in 1 BOTTLE (52959-030-40)

NDC Information of Cephalexin

NDC Code 52959-030-40
Proprietary Name Cephalexin
Package Description 40 CAPSULE in 1 BOTTLE (52959-030-40)
Product NDC 52959-030
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20051201
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name CEPHALEXIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cephalexin


General Information