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Levofloxacin - 23155-201-32 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 23155-201
Proprietary Name: Levofloxacin
Non Proprietary Name: Levofloxacin
Active Ingredient(s): 25    mg/mL & nbsp;   Levofloxacin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Levofloxacin

Product NDC: 23155-201
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202590
Marketing Category: ANDA
Start Marketing Date: 20130204

Package Information of Levofloxacin

Package NDC: 23155-201-32
Package Description: 1 VIAL, GLASS in 1 CARTON (23155-201-32) > 30 mL in 1 VIAL, GLASS

NDC Information of Levofloxacin

NDC Code 23155-201-32
Proprietary Name Levofloxacin
Package Description 1 VIAL, GLASS in 1 CARTON (23155-201-32) > 30 mL in 1 VIAL, GLASS
Product NDC 23155-201
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levofloxacin
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20130204
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc.
Substance Name LEVOFLOXACIN
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Levofloxacin


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