cephalexin - 50436-0117-4 - (cephalexin)

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Drug Information of cephalexin

Product NDC: 50436-0117
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: 50436-0117
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062791
Marketing Category: ANDA
Start Marketing Date: 20100621

Package Information of cephalexin

Package NDC: 50436-0117-4
Package Description: 14 CAPSULE in 1 BOTTLE (50436-0117-4)

NDC Information of cephalexin

NDC Code 50436-0117-4
Proprietary Name cephalexin
Package Description 14 CAPSULE in 1 BOTTLE (50436-0117-4)
Product NDC 50436-0117
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cephalexin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100621
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name CEPHALEXIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of cephalexin


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