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Levofloxacin - 33342-021-08 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 33342-021
Proprietary Name: Levofloxacin
Non Proprietary Name: Levofloxacin
Active Ingredient(s): 250    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: 33342-021
Labeler Name: Macleods Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200839
Marketing Category: ANDA
Start Marketing Date: 20120322

Package Information of Levofloxacin

Package NDC: 33342-021-08
Package Description: 50 TABLET, FILM COATED in 1 BOTTLE (33342-021-08)

NDC Information of Levofloxacin

NDC Code 33342-021-08
Proprietary Name Levofloxacin
Package Description 50 TABLET, FILM COATED in 1 BOTTLE (33342-021-08)
Product NDC 33342-021
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120322
Marketing Category Name ANDA
Labeler Name Macleods Pharmaceuticals Limited
Substance Name LEVOFLOXACIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Levofloxacin


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