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levofloxacin - 68382-017-01 - (levofloxacin)

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Drug Information of levofloxacin

Product NDC: 68382-017
Proprietary Name: levofloxacin
Non Proprietary Name: levofloxacin
Active Ingredient(s): 750    mg/1 & nbsp;   levofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of levofloxacin

Product NDC: 68382-017
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077652
Marketing Category: ANDA
Start Marketing Date: 20121110

Package Information of levofloxacin

Package NDC: 68382-017-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (68382-017-01)

NDC Information of levofloxacin

NDC Code 68382-017-01
Proprietary Name levofloxacin
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (68382-017-01)
Product NDC 68382-017
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121110
Marketing Category Name ANDA
Labeler Name Zydus Pharmaceuticals (USA) Inc.
Substance Name LEVOFLOXACIN
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of levofloxacin


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