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Levofloxacin - 55648-547-01 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 55648-547
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: 55648-547
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090367
Marketing Category: ANDA
Start Marketing Date: 20110620

Package Information of Levofloxacin

Package NDC: 55648-547-01
Package Description: 20 TABLET in 1 BOTTLE (55648-547-01)

NDC Information of Levofloxacin

NDC Code 55648-547-01
Proprietary Name Levofloxacin
Package Description 20 TABLET in 1 BOTTLE (55648-547-01)
Product NDC 55648-547
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levofloxacin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110620
Marketing Category Name ANDA
Labeler Name Wockhardt Limited
Substance Name LEVOFLOXACIN
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Levofloxacin


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