NDC 71335-0339

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 ID71335-0339_4a2678cc-4b3b-4592-8f3e-a5c57e497acd
NDC71335-0339
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 Strength750 mg/1
Pharm ClassesQuinolone Antimicrobial [EPC],Quinolones [CS]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 71335-0339-1

20 TABLET in 1 BOTTLE (71335-0339-1)
Marketing Start Date2013-04-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0339-1 [71335033901]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-04-25

NDC 71335-0339-3 [71335033903]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-04-25

NDC 71335-0339-2 [71335033902]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-04-25

NDC 71335-0339-5 [71335033905]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-04-25

NDC 71335-0339-4 [71335033904]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-04-25

NDC 71335-0339-7 [71335033907]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-04-25

NDC 71335-0339-6 [71335033906]

ciprofloxacin TABLET
Marketing CategoryANDA
Application NumberANDA076639
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-04-25

Drug Details

Active Ingredients

IngredientStrength
CIPROFLOXACIN HYDROCHLORIDE750 mg/1

OpenFDA Data

SPL SET ID:a5ecc693-b8fd-4a7a-8040-e56f801c9353
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.