Cephalexin - 52343-018-01 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 52343-018
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: 52343-018
Labeler Name: Gen-Source Rx
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090836
Marketing Category: ANDA
Start Marketing Date: 20111201

Package Information of Cephalexin

Package NDC: 52343-018-01
Package Description: 100 CAPSULE in 1 BOTTLE (52343-018-01)

NDC Information of Cephalexin

NDC Code 52343-018-01
Proprietary Name Cephalexin
Package Description 100 CAPSULE in 1 BOTTLE (52343-018-01)
Product NDC 52343-018
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20111201
Marketing Category Name ANDA
Labeler Name Gen-Source Rx
Substance Name CEPHALEXIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cephalexin


General Information