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Ciprofloxacin and Dextrose - 0409-4777-02 - (CIPROFLOXACIN)

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Drug Information of Ciprofloxacin and Dextrose

Product NDC: 0409-4777
Proprietary Name: Ciprofloxacin and Dextrose
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 and Dextrose

Product NDC: 0409-4777
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077753
Marketing Category: ANDA
Start Marketing Date: 20080318

Package Information of Ciprofloxacin and Dextrose

Package NDC: 0409-4777-02
Package Description: 24 BAG in 1 CASE (0409-4777-02) > 200 mL in 1 BAG

NDC Information of Ciprofloxacin and Dextrose

NDC Code 0409-4777-02
Proprietary Name Ciprofloxacin and Dextrose
Package Description 24 BAG in 1 CASE (0409-4777-02) > 200 mL in 1 BAG
Product NDC 0409-4777
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CIPROFLOXACIN
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20080318
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name CIPROFLOXACIN
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin and Dextrose


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