Cephalexin - 61442-162-30 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 61442-162
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: 61442-162
Labeler Name: Carlsbad Technology, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065152
Marketing Category: ANDA
Start Marketing Date: 20101015

Package Information of Cephalexin

Package NDC: 61442-162-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (61442-162-30)

NDC Information of Cephalexin

NDC Code 61442-162-30
Proprietary Name Cephalexin
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (61442-162-30)
Product NDC 61442-162
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101015
Marketing Category Name ANDA
Labeler Name Carlsbad Technology, 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