Cephalexin - 0143-9769-01 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 0143-9769
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: 0143-9769
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065444
Marketing Category: ANDA
Start Marketing Date: 20090901

Package Information of Cephalexin

Package NDC: 0143-9769-01
Package Description: 100 mL in 1 BOTTLE (0143-9769-01)

NDC Information of Cephalexin

NDC Code 0143-9769-01
Proprietary Name Cephalexin
Package Description 100 mL in 1 BOTTLE (0143-9769-01)
Product NDC 0143-9769
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 West-ward Pharmaceutical Corp
Substance Name CEPHALEXIN
Strength Number 125
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cephalexin


General Information