NDC 70518-2286

Ciprofloxacin

Ciprofloxacin Tablets

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

Product ID70518-2286_91243d01-2202-4d7a-e053-2a95a90a49d6
NDC70518-2286
Product TypeHuman Prescription Drug
Proprietary NameCiprofloxacin
Generic NameCiprofloxacin Tablets
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2019-08-27
Marketing CategoryANDA / ANDA
Application NumberANDA208921
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 70518-2286-1

14 TABLET, COATED in 1 BLISTER PACK (70518-2286-1)
Marketing Start Date2020-01-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70518-2286-1 [70518228601]

Ciprofloxacin TABLET, COATED
Marketing CategoryANDA
Application NumberANDA208921
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2020-01-10

NDC 70518-2286-0 [70518228600]

Ciprofloxacin TABLET, COATED
Marketing CategoryANDA
Application NumberANDA208921
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-08-27

NDC 70518-2286-2 [70518228602]

Ciprofloxacin TABLET, COATED
Marketing CategoryANDA
Application NumberANDA208921
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2020-02-11

Drug Details

Active Ingredients

IngredientStrength
CIPROFLOXACIN HYDROCHLORIDE500 mg/1

OpenFDA Data

SPL SET ID:d8b99e06-fc99-4751-88cf-25bf510035f3
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 Tablets"

    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.