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Levofloxacin - 0781-5790-10 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 0781-5790
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: 0781-5790
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077438
Marketing Category: ANDA
Start Marketing Date: 20110620

Package Information of Levofloxacin

Package NDC: 0781-5790-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (0781-5790-10)

NDC Information of Levofloxacin

NDC Code 0781-5790-10
Proprietary Name Levofloxacin
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (0781-5790-10)
Product NDC 0781-5790
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110620
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name LEVOFLOXACIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Levofloxacin


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