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Levofloxacin - 52125-060-02 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 52125-060
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: 52125-060
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201043
Marketing Category: ANDA
Start Marketing Date: 20130308

Package Information of Levofloxacin

Package NDC: 52125-060-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-060-02)

NDC Information of Levofloxacin

NDC Code 52125-060-02
Proprietary Name Levofloxacin
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-060-02)
Product NDC 52125-060
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130308
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LEVOFLOXACIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Levofloxacin


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