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Levofloxacin - 17478-106-10 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 17478-106
Proprietary Name: Levofloxacin
Non Proprietary Name: Levofloxacin
Active Ingredient(s): 5    mg/mL & nbsp;   Levofloxacin
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Levofloxacin

Product NDC: 17478-106
Labeler Name: Akorn Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090268
Marketing Category: ANDA
Start Marketing Date: 20110301

Package Information of Levofloxacin

Package NDC: 17478-106-10
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (17478-106-10) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of Levofloxacin

NDC Code 17478-106-10
Proprietary Name Levofloxacin
Package Description 1 BOTTLE, DROPPER in 1 CARTON (17478-106-10) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 17478-106
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levofloxacin
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20110301
Marketing Category Name ANDA
Labeler Name Akorn Inc.
Substance Name LEVOFLOXACIN
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Levofloxacin


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