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Levofloxacin - 0143-9720-01 - (Levofloxacin)

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Drug Information of Levofloxacin

Product NDC: 0143-9720
Proprietary Name: Levofloxacin
Non Proprietary Name: Levofloxacin
Active Ingredient(s): 750    mg/150mL & nbsp;   Levofloxacin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Levofloxacin

Product NDC: 0143-9720
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091375
Marketing Category: ANDA
Start Marketing Date: 20120131

Package Information of Levofloxacin

Package NDC: 0143-9720-01
Package Description: 24 POUCH in 1 CARTON (0143-9720-01) > 1 BAG in 1 POUCH > 150 mL in 1 BAG

NDC Information of Levofloxacin

NDC Code 0143-9720-01
Proprietary Name Levofloxacin
Package Description 24 POUCH in 1 CARTON (0143-9720-01) > 1 BAG in 1 POUCH > 150 mL in 1 BAG
Product NDC 0143-9720
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levofloxacin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120131
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
Substance Name LEVOFLOXACIN
Strength Number 750
Strength Unit mg/150mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Levofloxacin


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