LEVAQUIN - 50458-168-01 - (levofloxacin)

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Drug Information of LEVAQUIN

Product NDC: 50458-168
Proprietary Name: LEVAQUIN
Non Proprietary Name: levofloxacin
Active Ingredient(s): 5    mg/mL & nbsp;   levofloxacin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of LEVAQUIN

Product NDC: 50458-168
Labeler Name: Janssen Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020635
Marketing Category: NDA
Start Marketing Date: 19961220

Package Information of LEVAQUIN

Package NDC: 50458-168-01
Package Description: 100 mL in 1 BAG (50458-168-01)

NDC Information of LEVAQUIN

NDC Code 50458-168-01
Proprietary Name LEVAQUIN
Package Description 100 mL in 1 BAG (50458-168-01)
Product NDC 50458-168
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levofloxacin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19961220
Marketing Category Name NDA
Labeler Name Janssen Pharmaceuticals, Inc.
Substance Name LEVOFLOXACIN
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of LEVAQUIN


General Information