Moxifloxacin PF

Manufacturer: ImprimisRx NJ | Imprimis Pharmaceuticals
Effective date: 2018-05-08
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 20:25:43

Label at a glance#

ProductMoxifloxacin PF

Active ingredientMOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE

Label structure2 sections

Storage and handling

Store at 20° to 25° C (68° to 77° F)

Label contents#

Full prescribing information#

STORAGE AND HANDLING SECTION

Store at 20° to 25° C (68° to 77° F)

Vial Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Vial Label

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
MOXIFLOXACIN Pharmacologic Class Indexing	3	Indexing - Pharmacologic Class	20230421

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
84b851da-be59-d750-14d1-e4d93cc3b4da	Product name	9	20250630
2194a6ab-15bb-de49-cced-f09e642b1b64	Product name	8	20240313
d7840f4c-f22a-4403-b5da-53ac6ac8fd90	Product name	1	20150728
ccc7bb05-654a-45d2-a0d6-09ab96ba531b	Product name	2	20150611

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70261-511-01	2020-01-31	C162847	48780-1	9d75b9d0-3184-f424-e053-dadaa90a57ce	6bb744c0-b612-2858-e053-2991aa0ae715

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70261-511-01	Moxifloxacin PF	1 mL in 1 VIAL, GLASS	INJECTION, SOLUTION	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70261-511	MOXIFLOXACIN PF INJECTION, SOLUTION [IMPRIMISRX NJ]	1	Legacy NDC, 1 package rows	20180509_6bb744c0-b612-2858-e053-2991aa0ae715.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Moxifloxacin PF
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE
MOXIFLOXACIN
SODIUM CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70261-511	70261-511-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE	B8956S8609	ACTIM
SODIUM CHLORIDE	451W47IQ8X	IACT

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
6bb744c0-b613-2858-e053-2991aa0ae715			6bb744c0-b612-2858-e053-2991aa0ae715	2018-05-08		Exact identifier spl id: 6bb744c0-b613-2858-e053-2991aa0ae715 spl set id: 6bb744c0-b612-2858-e053-2991aa0ae715

Reported adverse events (FAERS/openFDA)#

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