cephalexin - 68180-124-02 - (Cephalexin)

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Drug Information of cephalexin

Product NDC: 68180-124
Proprietary Name: cephalexin
Non Proprietary Name: Cephalexin
Active Ingredient(s): 250    mg/5mL & nbsp;   Cephalexin
Administration Route(s): ORAL
Dosage Form(s): FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of cephalexin

Product NDC: 68180-124
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065234
Marketing Category: ANDA
Start Marketing Date: 20060111

Package Information of cephalexin

Package NDC: 68180-124-02
Package Description: 200 mL in 1 BOTTLE (68180-124-02)

NDC Information of cephalexin

NDC Code 68180-124-02
Proprietary Name cephalexin
Package Description 200 mL in 1 BOTTLE (68180-124-02)
Product NDC 68180-124
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20060111
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, Inc.
Substance Name CEPHALEXIN
Strength Number 250
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of cephalexin


General Information