NDC 70518-0010

ciprofloxacin

Ciprofloxacin

ciprofloxacin is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Ciprofloxacin Hydrochloride.

Product ID70518-0010_814f68f1-4d42-6ddb-e053-2991aa0a2aec
NDC70518-0010
Product TypeHuman Prescription Drug
Proprietary Nameciprofloxacin
Generic NameCiprofloxacin
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-11-21
Marketing CategoryANDA / ANDA
Application NumberANDA076639
Labeler NameREMEDYREPACK INC.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Active Ingredient Strength500 mg/1
Pharm ClassesQuinolone Antimicrobial [EPC],Quinolones [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 70518-0010-5

10 TABLET in 1 BOTTLE, PLASTIC (70518-0010-5)
Marketing Start Date2017-03-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70518-0010-0 [70518001000]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-21
Marketing End Date2019-06-28

NDC 70518-0010-4 [70518001004]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-01-18
Marketing End Date2019-05-01

NDC 70518-0010-2 [70518001002]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-30
Marketing End Date2019-07-12

NDC 70518-0010-3 [70518001003]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-01-13
Marketing End Date2018-09-14

NDC 70518-0010-1 [70518001001]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-21
Marketing End Date2018-11-25

NDC 70518-0010-5 [70518001005]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-02
Marketing End Date2019-08-03

Drug Details

Active Ingredients

IngredientStrength
CIPROFLOXACIN HYDROCHLORIDE500 mg/1

OpenFDA Data

SPL SET ID:fe90cd58-b243-490e-9c25-15338b6dad9d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 309309
  • Pharmacological Class

    • Quinolone Antimicrobial [EPC]
    • Quinolones [CS]

    NDC Crossover Matching brand name "ciprofloxacin" or generic name "Ciprofloxacin"

    NDCBrand NameGeneric Name
    0143-2037CiprofloxacinCiprofloxacin
    0143-9927CiprofloxacinCiprofloxacin
    0143-9928CiprofloxacinCiprofloxacin
    0143-9929CiprofloxacinCiprofloxacin
    0172-5312CiprofloxacinCiprofloxacin
    0179-0188CiprofloxacinCiprofloxacin
    0378-1743Ciprofloxacinciprofloxacin
    0378-1745Ciprofloxacinciprofloxacin
    0378-7098Ciprofloxacinciprofloxacin
    0404-7187CiprofloxacinCiprofloxacin Hydrochloride
    0409-4777CIPROFLOXACINCIPROFLOXACIN
    0440-6290CiprofloxacinCiprofloxacin Hydrochloride
    0440-6291CiprofloxacinCiprofloxacin Hydrochloride
    68071-1530CiprofloxacinCiprofloxacin
    68071-1616CiprofloxacinCiprofloxacin
    68071-1893ciprofloxacinciprofloxacin
    68071-3013ciprofloxacinciprofloxacin
    68071-4201ciprofloxacinciprofloxacin
    68071-4122ciprofloxacinciprofloxacin
    68071-4387CiprofloxacinCiprofloxacin
    68071-4492CiprofloxacinCiprofloxacin
    68071-4260ciprofloxacinciprofloxacin
    68071-4403CiprofloxacinCiprofloxacin
    68071-4679ciprofloxacinciprofloxacin
    68071-4576CiprofloxacinCiprofloxacin
    68071-4813CiprofloxacinCiprofloxacin
    68071-4627CiprofloxacinCiprofloxacin
    68084-071CiprofloxacinCiprofloxacin
    68084-070CiprofloxacinCiprofloxacin
    68071-4672ciprofloxacinciprofloxacin
    68084-069CiprofloxacinCiprofloxacin
    68180-392CIPROFLOXACINCIPROFLOXACIN
    68180-393CIPROFLOXACINCIPROFLOXACIN
    68645-060CiprofloxacinCiprofloxacin
    68788-9012ciprofloxacinciprofloxacin
    68788-9330CiprofloxacinCiprofloxacin
    68788-9006CiprofloxacinCiprofloxacin
    68788-9280ciprofloxacinciprofloxacin
    68788-9228CiprofloxacinCiprofloxacin
    68788-9024CiprofloxacinCiprofloxacin
    68788-9944CiprofloxacinCiprofloxacin
    68788-9724CiprofloxacinCiprofloxacin
    68788-9391CiprofloxacinCiprofloxacin
    69117-0008CiprofloxacinCiprofloxacin
    69117-0009CiprofloxacinCiprofloxacin
    69315-308ciprofloxacinciprofloxacin
    70518-0010ciprofloxacinciprofloxacin
    70518-0464ciprofloxacinciprofloxacin
    70518-0340CiprofloxacinCiprofloxacin
    70518-0368ciprofloxacinciprofloxacin

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.