NDC 63629-5154

ciprofloxacin

Ciprofloxacin

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

Product ID63629-5154_76459371-f268-446a-882c-97b47df21e3a
NDC63629-5154
Product TypeHuman Prescription Drug
Proprietary Nameciprofloxacin
Generic NameCiprofloxacin
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2004-09-10
Marketing CategoryANDA / ANDA
Application NumberANDA076639
Labeler NameBryant Ranch Prepack
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Active Ingredient Strength500 mg/1
Pharm ClassesQuinolone Antimicrobial [EPC],Quinolones [CS]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 63629-5154-1

10 TABLET in 1 BOTTLE (63629-5154-1)
Marketing Start Date2006-01-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-5154-3 [63629515403]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-24
Inactivation Date2020-01-31

NDC 63629-5154-4 [63629515404]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-24
Inactivation Date2020-01-31

NDC 63629-5154-2 [63629515402]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-24
Inactivation Date2020-01-31

NDC 63629-5154-5 [63629515405]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-24
Inactivation Date2020-01-31

NDC 63629-5154-7 [63629515407]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-24
Inactivation Date2020-01-31

NDC 63629-5154-1 [63629515401]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-24
Inactivation Date2020-01-31

NDC 63629-5154-6 [63629515406]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-01-24
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CIPROFLOXACIN HYDROCHLORIDE500 mg/1

OpenFDA Data

SPL SET ID:f23a7533-839e-416d-b668-030f0213f337
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
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