NDC 0065-0656

Ciloxan

Ciprofloxacin Hydrochloride

Ciloxan is a Ophthalmic Solution/ Drops in the Human Prescription Drug category. It is labeled and distributed by Alcon Laboratories, Inc.. The primary component is Ciprofloxacin Hydrochloride.

Product ID0065-0656_0b3a3acd-dc13-403e-a8b1-761de56a476a
NDC0065-0656
Product TypeHuman Prescription Drug
Proprietary NameCiloxan
Generic NameCiprofloxacin Hydrochloride
Dosage FormSolution/ Drops
Route of AdministrationOPHTHALMIC
Marketing Start Date1991-01-15
Marketing End Date2023-04-30
Marketing CategoryNDA / NDA
Application NumberNDA019992
Labeler NameAlcon Laboratories, Inc.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Active Ingredient Strength3 mg/mL
Pharm ClassesQuinolone Antimicrobial [EPC], Quinolones [CS]
NDC Exclude FlagN

Packaging

NDC 0065-0656-05

1 BOTTLE, PLASTIC in 1 CARTON (0065-0656-05) > 5 mL in 1 BOTTLE, PLASTIC
Marketing Start Date1991-01-15
Marketing End Date2023-04-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0065-0656-10 [00065065610]

Ciloxan SOLUTION/ DROPS
Marketing CategoryNDA
Application NumberNDA019992
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-01-15

NDC 0065-0656-01 [00065065601]

Ciloxan SOLUTION/ DROPS
Marketing CategoryNDA
Application NumberNDA019992
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-01-15
Marketing End Date2011-07-28

NDC 0065-0656-11 [00065065611]

Ciloxan SOLUTION/ DROPS
Marketing CategoryNDA
Application NumberNDA019992
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-01-15
Marketing End Date2011-07-28

NDC 0065-0656-05 [00065065605]

Ciloxan SOLUTION/ DROPS
Marketing CategoryNDA
Application NumberNDA019992
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1991-01-15

NDC 0065-0656-25 [00065065625]

Ciloxan SOLUTION/ DROPS
Marketing CategoryNDA
Application NumberNDA019992
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-01-15

Drug Details

Active Ingredients

IngredientStrength
CIPROFLOXACIN HYDROCHLORIDE3 mg/mL

OpenFDA Data

SPL SET ID:614af481-f9ef-44ac-9cb8-f421660d9cdd
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 309307
  • 103943

    • Pharmacological Class

    • Quinolone Antimicrobial [EPC]
    • Quinolones [CS]

    NDC Crossover Matching brand name "Ciloxan" or generic name "Ciprofloxacin Hydrochloride"

    NDCBrand NameGeneric Name
    0065-0654CILOXANciprofloxacin hydrochloride
    0065-0656Ciloxanciprofloxacin hydrochloride
    0078-0841CILOXANciprofloxacin hydrochloride
    70518-1234CiloxanCiloxan
    0404-7187CiprofloxacinCiprofloxacin Hydrochloride
    0440-6290CiprofloxacinCiprofloxacin Hydrochloride
    0440-6291CiprofloxacinCiprofloxacin Hydrochloride
    11819-323Ciprofloxacinciprofloxacin hydrochloride
    11819-351Ciprofloxacinciprofloxacin hydrochloride
    11819-360CiprofloxacinCIPROFLOXACIN HYDROCHLORIDE
    16571-120CiprofloxacinCIPROFLOXACIN HYDROCHLORIDE
    16714-651CiprofloxacinCiprofloxacin Hydrochloride
    16714-652CiprofloxacinCiprofloxacin Hydrochloride
    16714-653CiprofloxacinCiprofloxacin Hydrochloride
    17478-714CiprofloxacinCiprofloxacin Hydrochloride
    21695-210Ciprofloxacinciprofloxacin hydrochloride
    10544-606Ciprofloxacin hydrochlorideCiprofloxacin hydrochloride
    21695-259Ciprofloxacin Hydrochlorideciprofloxacin hydrochloride
    13913-001Proquinciprofloxacin hydrochloride

    Trademark Results [Ciloxan]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    CILOXAN
    CILOXAN
    74105467 1717026 Live/Registered
    NOVARTIS AG
    1990-10-12
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.