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Ciprofloxacin - 17478-714-25 - (Ciprofloxacin Hydrochloride)

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Drug Information of Ciprofloxacin

Product NDC: 17478-714
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin Hydrochloride
Active Ingredient(s): 3    mg/mL & nbsp;   Ciprofloxacin Hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 17478-714
Labeler Name: Akorn Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076555
Marketing Category: ANDA
Start Marketing Date: 20090724

Package Information of Ciprofloxacin

Package NDC: 17478-714-25
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (17478-714-25) > 2.5 mL in 1 BOTTLE, DROPPER

NDC Information of Ciprofloxacin

NDC Code 17478-714-25
Proprietary Name Ciprofloxacin
Package Description 1 BOTTLE, DROPPER in 1 CARTON (17478-714-25) > 2.5 mL in 1 BOTTLE, DROPPER
Product NDC 17478-714
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin Hydrochloride
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20090724
Marketing Category Name ANDA
Labeler Name Akorn Inc.
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


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