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Levofloxacin - 65862-538-10 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 65862-538
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: 65862-538
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201043
Marketing Category: ANDA
Start Marketing Date: 20110620

Package Information of Levofloxacin

Package NDC: 65862-538-10
Package Description: 10 BLISTER PACK in 1 CARTON (65862-538-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Levofloxacin

NDC Code 65862-538-10
Proprietary Name Levofloxacin
Package Description 10 BLISTER PACK in 1 CARTON (65862-538-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 65862-538
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 Aurobindo Pharma Limited
Substance Name LEVOFLOXACIN
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Levofloxacin


General Information