Cephalexin - 76439-101-10 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 76439-101
Proprietary Name: Cephalexin
Non Proprietary Name: Cephalexin
Active Ingredient(s): 250    mg/1 & nbsp;   Cephalexin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Cephalexin

Product NDC: 76439-101
Labeler Name: Virtus Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062713
Marketing Category: ANDA
Start Marketing Date: 20120112

Package Information of Cephalexin

Package NDC: 76439-101-10
Package Description: 100 CAPSULE in 1 BOTTLE (76439-101-10)

NDC Information of Cephalexin

NDC Code 76439-101-10
Proprietary Name Cephalexin
Package Description 100 CAPSULE in 1 BOTTLE (76439-101-10)
Product NDC 76439-101
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120112
Marketing Category Name ANDA
Labeler Name Virtus Pharmaceuticals, LLC
Substance Name CEPHALEXIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cephalexin


General Information