Cephalexin - 68180-122-01 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 68180-122
Proprietary Name: Cephalexin
Non Proprietary Name: Cephalexin
Active Ingredient(s): 500    mg/1 & nbsp;   Cephalexin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Cephalexin

Product NDC: 68180-122
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065229
Marketing Category: ANDA
Start Marketing Date: 20060111

Package Information of Cephalexin

Package NDC: 68180-122-01
Package Description: 100 CAPSULE in 1 BOTTLE (68180-122-01)

NDC Information of Cephalexin

NDC Code 68180-122-01
Proprietary Name Cephalexin
Package Description 100 CAPSULE in 1 BOTTLE (68180-122-01)
Product NDC 68180-122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20060111
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, Inc.
Substance Name CEPHALEXIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cephalexin


General Information