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Ciprofloxacin Hydrochloride - 61314-656-25 - (Ciprofloxacin Hydrochloride)

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Drug Information of Ciprofloxacin Hydrochloride

Product NDC: 61314-656
Proprietary Name: Ciprofloxacin Hydrochloride
Non Proprietary Name: Ciprofloxacin Hydrochloride
Active Ingredient(s): 3.5    mg/mL & nbsp;   Ciprofloxacin Hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin Hydrochloride

Product NDC: 61314-656
Labeler Name: Falcon Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019992
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20040507

Package Information of Ciprofloxacin Hydrochloride

Package NDC: 61314-656-25
Package Description: 2.5 mL in 1 BOTTLE, PLASTIC (61314-656-25)

NDC Information of Ciprofloxacin Hydrochloride

NDC Code 61314-656-25
Proprietary Name Ciprofloxacin Hydrochloride
Package Description 2.5 mL in 1 BOTTLE, PLASTIC (61314-656-25)
Product NDC 61314-656
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin Hydrochloride
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20040507
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Falcon Pharmaceuticals, Ltd.
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 3.5
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin Hydrochloride


General Information