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Levofloxacin - 59115-097-55 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 59115-097
Proprietary Name: Levofloxacin
Non Proprietary Name: Levofloxacin
Active Ingredient(s): 750    mg/1 & nbsp;   Levofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Levofloxacin

Product NDC: 59115-097
Labeler Name: Hikma Pharmaceutical
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078767
Marketing Category: ANDA
Start Marketing Date: 20110621

Package Information of Levofloxacin

Package NDC: 59115-097-55
Package Description: 500 TABLET in 1 BOTTLE (59115-097-55)

NDC Information of Levofloxacin

NDC Code 59115-097-55
Proprietary Name Levofloxacin
Package Description 500 TABLET in 1 BOTTLE (59115-097-55)
Product NDC 59115-097
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levofloxacin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110621
Marketing Category Name ANDA
Labeler Name Hikma Pharmaceutical
Substance Name LEVOFLOXACIN
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Levofloxacin


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