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Levofloxacin - 59762-0278-2 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 59762-0278
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: 59762-0278
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201043
Marketing Category: ANDA
Start Marketing Date: 20110620

Package Information of Levofloxacin

Package NDC: 59762-0278-2
Package Description: 50 TABLET, FILM COATED in 1 BOTTLE (59762-0278-2)

NDC Information of Levofloxacin

NDC Code 59762-0278-2
Proprietary Name Levofloxacin
Package Description 50 TABLET, FILM COATED in 1 BOTTLE (59762-0278-2)
Product NDC 59762-0278
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 Greenstone LLC
Substance Name LEVOFLOXACIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Levofloxacin


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