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Ciprofloxacin - 36000-009-24 - (Ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 36000-009
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin
Active Ingredient(s): 2    mg/mL & nbsp;   Ciprofloxacin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 36000-009
Labeler Name: Claris Lifesciences Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078024
Marketing Category: ANDA
Start Marketing Date: 20080804

Package Information of Ciprofloxacin

Package NDC: 36000-009-24
Package Description: 200 mL in 1 BAG (36000-009-24)

NDC Information of Ciprofloxacin

NDC Code 36000-009-24
Proprietary Name Ciprofloxacin
Package Description 200 mL in 1 BAG (36000-009-24)
Product NDC 36000-009
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20080804
Marketing Category Name ANDA
Labeler Name Claris Lifesciences Inc.
Substance Name CIPROFLOXACIN
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


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