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Levofloxacin - 68788-9707-1 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 68788-9707
Proprietary Name: Levofloxacin
Non Proprietary Name: Levofloxacin
Active Ingredient(s): 500    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: 68788-9707
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201043
Marketing Category: ANDA
Start Marketing Date: 20130129

Package Information of Levofloxacin

Package NDC: 68788-9707-1
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE (68788-9707-1)

NDC Information of Levofloxacin

NDC Code 68788-9707-1
Proprietary Name Levofloxacin
Package Description 10 TABLET, FILM COATED in 1 BOTTLE (68788-9707-1)
Product NDC 68788-9707
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130129
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
Substance Name LEVOFLOXACIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Levofloxacin


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