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Ciprofloxacin - 0781-3240-09 - (Ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 0781-3240
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin
Active Ingredient(s): 2    mg/mL & nbsp;   Ciprofloxacin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 0781-3240
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078252
Marketing Category: ANDA
Start Marketing Date: 20080324

Package Information of Ciprofloxacin

Package NDC: 0781-3240-09
Package Description: 24 POUCH in 1 CARTON (0781-3240-09) > 1 BAG in 1 POUCH (0781-3240-48) > 200 mL in 1 BAG

NDC Information of Ciprofloxacin

NDC Code 0781-3240-09
Proprietary Name Ciprofloxacin
Package Description 24 POUCH in 1 CARTON (0781-3240-09) > 1 BAG in 1 POUCH (0781-3240-48) > 200 mL in 1 BAG
Product NDC 0781-3240
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20080324
Marketing Category Name ANDA
Labeler Name Sandoz 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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