Cephalexin - 0093-4177-74 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 0093-4177
Proprietary Name: Cephalexin
Non Proprietary Name: Cephalexin
Active Ingredient(s): 250    mg/5mL & nbsp;   Cephalexin
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Cephalexin

Product NDC: 0093-4177
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062703
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Cephalexin

Package NDC: 0093-4177-74
Package Description: 200 mL in 1 BOTTLE (0093-4177-74)

NDC Information of Cephalexin

NDC Code 0093-4177-74
Proprietary Name Cephalexin
Package Description 200 mL in 1 BOTTLE (0093-4177-74)
Product NDC 0093-4177
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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