Cephalexin - 68289-008-20 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 68289-008
Proprietary Name: Cephalexin
Non Proprietary Name: Cephalexin
Active Ingredient(s): 125    mg/5mL & nbsp;   Cephalexin
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Cephalexin

Product NDC: 68289-008
Labeler Name: Jazeera Pharmaceutical
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065444
Marketing Category: ANDA
Start Marketing Date: 20090901

Package Information of Cephalexin

Package NDC: 68289-008-20
Package Description: 200 mL in 1 BOTTLE (68289-008-20)

NDC Information of Cephalexin

NDC Code 68289-008-20
Proprietary Name Cephalexin
Package Description 200 mL in 1 BOTTLE (68289-008-20)
Product NDC 68289-008
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20090901
Marketing Category Name ANDA
Labeler Name Jazeera Pharmaceutical
Substance Name CEPHALEXIN ANHYDROUS
Strength Number 125
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cephalexin


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