Cephalexin - 68788-9950-2 - (Cephalexin)

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Drug Information of Cephalexin

Product NDC: 68788-9950
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: 68788-9950
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065248
Marketing Category: ANDA
Start Marketing Date: 20120305

Package Information of Cephalexin

Package NDC: 68788-9950-2
Package Description: 20 CAPSULE in 1 BOTTLE, PLASTIC (68788-9950-2)

NDC Information of Cephalexin

NDC Code 68788-9950-2
Proprietary Name Cephalexin
Package Description 20 CAPSULE in 1 BOTTLE, PLASTIC (68788-9950-2)
Product NDC 68788-9950
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cephalexin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120305
Marketing Category Name ANDA
Labeler Name Preferred 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