Ciprofloxacin HCl

Manufacturer: AX Pharmaceutical Corp
Effective date: 2019-11-11
Label type: BULK INGREDIENT
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-02 00:02:05

Label at a glance#

ProductCiprofloxacin HCl

Active ingredientCIPROFLOXACIN HYDROCHLORIDE

Label structure1 sections

Label contents#

Full prescribing information#

Ciprofloxacin HCl

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

Ciprofloxacin HCl
CIPROFLOXACIN HYDROCHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62157-928	62157-928-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CIPROFLOXACIN HYDROCHLORIDE	4BA73M5E37	ACTIM

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 4 of 4 · 63 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ciprofloxacin Hydrochloride	CIPROFLOXACIN HYDROCHLORIDE	Sandoz Inc	ab52b14d-345b-47ff-a832-465caddd3801	2019-07-18	Warnings, Adverse reactions	Name fallback generic name: CIPROFLOXACIN HYDROCHLORIDE
Ciprofloxacin	CIPROFLOXACIN HYDROCHLORIDE	Aphena Pharma Solutions - Tennessee, LLC	df24efa3-c9a0-4f40-92ce-cc71c708931b	2018-10-31	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: CIPROFLOXACIN HYDROCHLORIDE
Ciprofloxacin	CIPROFLOXACIN HYDROCHLORIDE	Aphena Pharma Solutions - Tennessee, LLC	4e74496f-4dca-4471-be32-c0a14bc62750	2018-10-16	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: CIPROFLOXACIN HYDROCHLORIDE

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.