Ciprofloxacin

Product NDC
71335-2450
11-digit product format
713352450
Labeler code
71335
Product ID
71335-2450_a5fcba51-4ab6-4b4a-a73d-64dec62a2e52
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ciprofolxacin
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA208921
Marketing category
ANDA
Marketing start
2023-10-01
Substance
CIPROFLOXACIN HYDROCHLORIDE
Active strength
500 mg/1
Pharmacologic classes
Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
4BA73M5E37CIPROFLOXACIN HYDROCHLORIDE86393-32-0CIPROFLOXACIN HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2450-0713352450007 TABLET in 1 BOTTLE (71335-2450-0) 7 tablet2024-08-15NoNoHistorical
71335-2450-17133524500114 TABLET in 1 BOTTLE (71335-2450-1) 14 tablet2024-08-15NoNoHistorical
71335-2450-27133524500230 TABLET in 1 BOTTLE (71335-2450-2) 30 tablet2024-08-15NoNoHistorical
71335-2450-37133524500320 TABLET in 1 BOTTLE (71335-2450-3) 20 tablet2024-08-15NoNoHistorical
71335-2450-47133524500460 TABLET in 1 BOTTLE (71335-2450-4) 60 tablet2024-08-15NoNoHistorical
71335-2450-5713352450056 TABLET in 1 BOTTLE (71335-2450-5) 6 tablet2024-08-15NoNoHistorical
71335-2450-67133524500610 TABLET in 1 BOTTLE (71335-2450-6) 10 tablet2024-08-15NoNoHistorical
71335-2450-77133524500728 TABLET in 1 BOTTLE (71335-2450-7) 28 tablet2024-08-15NoNoHistorical
71335-2450-871335245008100 TABLET in 1 BOTTLE (71335-2450-8) 100 tablet2024-08-15NoNoHistorical
71335-2450-97133524500940 TABLET in 1 BOTTLE (71335-2450-9) 40 tablet2024-08-15NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CiprofloxacinBryant Ranch Prepack2024-08-15HUMAN PRESCRIPTION DRUG LABEL2