NDC 63304-711

Ciprofloxacin

Ciprofloxacin

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

Product ID63304-711_aa0b6a4a-f8ff-4d09-8813-2d58192c08c5
NDC63304-711
Product TypeHuman Prescription Drug
Proprietary NameCiprofloxacin
Generic NameCiprofloxacin
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2004-06-09
Marketing CategoryANDA / ANDA
Application NumberANDA075747
Labeler NameRanbaxy Pharmaceuticals Inc.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Active Ingredient Strength750 mg/1
Pharm ClassesQuinolone Antimicrobial [EPC],Quinolones [CS]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 63304-711-50

50 TABLET, FILM COATED in 1 BOTTLE (63304-711-50)
Marketing Start Date2004-06-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63304-711-01 [63304071101]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075747
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-06-09
Inactivation Date2019-11-27

NDC 63304-711-80 [63304071180]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075747
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-06-09
Inactivation Date2019-11-27

NDC 63304-711-05 [63304071105]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075747
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-06-09
Inactivation Date2019-11-27

NDC 63304-711-13 [63304071113]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075747
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-06-09
Marketing End Date2013-03-12

NDC 63304-711-14 [63304071114]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075747
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-06-09
Inactivation Date2019-11-27

NDC 63304-711-50 [63304071150]

Ciprofloxacin TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075747
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-06-09
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
CIPROFLOXACIN HYDROCHLORIDE750 mg/1

OpenFDA Data

SPL SET ID:563e576e-6966-4f8d-91bb-0a1a951de324
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"

    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.