NDC 52959-730

Ciprofloxacin

Ciprofloxacin Hydrochloride

Ciprofloxacin is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by H.j. Harkins Company, Inc.. The primary component is Ciprofloxacin Hydrochloride.

Product ID52959-730_9adbd7e3-4ea3-4ef7-8112-a6a0c31b4b6a
NDC52959-730
Product TypeHuman Prescription Drug
Proprietary NameCiprofloxacin
Generic NameCiprofloxacin Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2004-06-09
Marketing CategoryANDA / ANDA
Application NumberANDA076794
Labeler NameH.J. Harkins Company, Inc.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Active Ingredient Strength500 mg/1
Pharm ClassesQuinolone Antimicrobial [EPC],Quinolones [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 52959-730-28

28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52959-730-28)
Marketing Start Date2004-06-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52959-730-20 [52959073020]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076794
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-06-09
Inactivation Date2019-11-13

NDC 52959-730-15 [52959073015]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076794
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-06-09
Inactivation Date2019-11-13

NDC 52959-730-00 [52959073000]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076794
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-06-09
Inactivation Date2019-11-13

NDC 52959-730-30 [52959073030]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076794
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-06-09
Inactivation Date2019-11-13

NDC 52959-730-06 [52959073006]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076794
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-06-09
Inactivation Date2019-11-13

NDC 52959-730-28 [52959073028]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076794
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-06-09
Inactivation Date2019-11-13

NDC 52959-730-60 [52959073060]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076794
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-06-09
Inactivation Date2019-11-13

NDC 52959-730-10 [52959073010]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076794
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-06-09
Inactivation Date2019-11-13

NDC 52959-730-04 [52959073004]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076794
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-06-09
Inactivation Date2019-11-13

NDC 52959-730-21 [52959073021]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076794
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-06-09
Inactivation Date2019-11-13

NDC 52959-730-14 [52959073014]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076794
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-06-09
Inactivation Date2019-11-13

Drug Details

Active Ingredients

IngredientStrength
CIPROFLOXACIN HYDROCHLORIDE500 mg/1

OpenFDA Data

SPL SET ID:99a81fda-81dc-40b3-b55a-165b6e4ca4ee
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 309309
  • 197512
  • 197511

    • Pharmacological Class

    • Quinolone Antimicrobial [EPC]
    • Quinolones [CS]

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

    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
    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
    70518-1278CiprofloxacinCiprofloxacin
    70518-0522CiprofloxacinCiprofloxacin
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