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Levofloxacin - 54868-6279-2 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 54868-6279
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: 54868-6279
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076710
Marketing Category: ANDA
Start Marketing Date: 20110622

Package Information of Levofloxacin

Package NDC: 54868-6279-2
Package Description: 7 TABLET, FILM COATED in 1 BOTTLE (54868-6279-2)

NDC Information of Levofloxacin

NDC Code 54868-6279-2
Proprietary Name Levofloxacin
Package Description 7 TABLET, FILM COATED in 1 BOTTLE (54868-6279-2)
Product NDC 54868-6279
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110622
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name LEVOFLOXACIN
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Levofloxacin


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