Ciloxan - 0065-0656-25 - (ciprofloxacin hydrochloride)

Alphabetical Index


Drug Information of Ciloxan

Product NDC: 0065-0656
Proprietary Name: Ciloxan
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 Ciloxan

Product NDC: 0065-0656
Labeler Name: Alcon Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019992
Marketing Category: NDA
Start Marketing Date: 19910115

Package Information of Ciloxan

Package NDC: 0065-0656-25
Package Description: 2.5 mL in 1 BOTTLE, PLASTIC (0065-0656-25)

NDC Information of Ciloxan

NDC Code 0065-0656-25
Proprietary Name Ciloxan
Package Description 2.5 mL in 1 BOTTLE, PLASTIC (0065-0656-25)
Product NDC 0065-0656
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin hydrochloride
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 19910115
Marketing Category Name NDA
Labeler Name Alcon Laboratories, Inc.
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 3.5
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciloxan


General Information