Cephalexin - 21695-789-20 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 21695-789
Proprietary Name: Cephalexin
Non Proprietary Name: Cephalexin
Active Ingredient(s): 125    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: 21695-789
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062703
Marketing Category: ANDA
Start Marketing Date: 20100921

Package Information of Cephalexin

Package NDC: 21695-789-20
Package Description: 200 mL in 1 BOTTLE (21695-789-20)

NDC Information of Cephalexin

NDC Code 21695-789-20
Proprietary Name Cephalexin
Package Description 200 mL in 1 BOTTLE (21695-789-20)
Product NDC 21695-789
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20100921
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name CEPHALEXIN
Strength Number 125
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Cephalexin


General Information