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Ciprofloxacin - 21695-422-01 - (Ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 21695-422
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin
Active Ingredient(s): 10    mg/mL & nbsp;   Ciprofloxacin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 21695-422
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077782
Marketing Category: ANDA
Start Marketing Date: 20060828

Package Information of Ciprofloxacin

Package NDC: 21695-422-01
Package Description: 20 mL in 1 VIAL (21695-422-01)

NDC Information of Ciprofloxacin

NDC Code 21695-422-01
Proprietary Name Ciprofloxacin
Package Description 20 mL in 1 VIAL (21695-422-01)
Product NDC 21695-422
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20060828
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name CIPROFLOXACIN
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


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