Ciprofloxacin

Product NDC
72162-1741
11-digit product format
721621741
Labeler code
72162
Product ID
72162-1741_d2a899a6-43fe-42f7-b1b5-4731f74e3792
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ciprofloxacin Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA076126
Marketing category
ANDA
Marketing start
2009-10-10
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 formatDescriptionMarketing startSampleExclude flagStatus
72162-1741-172162174101100 TABLET, FILM COATED in 1 BOTTLE (72162-1741-1) 2024-10-04NoNoHistorical
72162-1741-27216217410214 TABLET, FILM COATED in 1 BOTTLE (72162-1741-2) 2024-10-04NoNoHistorical
72162-1741-37216217410330 TABLET, FILM COATED in 1 BOTTLE (72162-1741-3) 2024-10-04NoNoHistorical
72162-1741-47216217410420 TABLET, FILM COATED in 1 BOTTLE (72162-1741-4) 2024-10-04NoNoHistorical
72162-1741-572162174105500 TABLET, FILM COATED in 1 BOTTLE (72162-1741-5) 2024-10-04NoNoHistorical
72162-1741-67216217410660 TABLET, FILM COATED in 1 BOTTLE (72162-1741-6) 2024-10-04NoNoHistorical
72162-1741-77216217410710 TABLET, FILM COATED in 1 BOTTLE (72162-1741-7) 2024-10-04NoNoHistorical
72162-1741-872162174108120 TABLET, FILM COATED in 1 BOTTLE (72162-1741-8) 2024-10-04NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CiprofloxacinBryant Ranch Prepack2025-04-01HUMAN PRESCRIPTION DRUG LABEL106