Cephalexin - 35356-978-14 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 35356-978
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: 35356-978
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090836
Marketing Category: ANDA
Start Marketing Date: 20110120

Package Information of Cephalexin

Package NDC: 35356-978-14
Package Description: 14 CAPSULE in 1 BOTTLE (35356-978-14)

NDC Information of Cephalexin

NDC Code 35356-978-14
Proprietary Name Cephalexin
Package Description 14 CAPSULE in 1 BOTTLE (35356-978-14)
Product NDC 35356-978
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110120
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name CEPHALEXIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cephalexin


General Information