FDA.reportPublic FDA data

Triamcinolone-Moxifloxacin PF

Manufacturer
Imprimis NJOF, LLC
Effective date
2020-02-10
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 20:32:15

Label at a glance#

ProductTriamcinolone-Moxifloxacin PF
Active ingredientTRIAMCINOLONE ACETONIDE, MOXIFLOXACIN 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)

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
MOXIFLOXACIN Pharmacologic Class Indexing3Indexing - Pharmacologic Class20230421
TRIAMCINOLONE ACETONIDE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d4d7da1a-7fd4-628e-cdae-89e749b1c534Product name720260127
75f7e47b-8736-a182-fc44-22aca8d79689Product name220251211
84b851da-be59-d750-14d1-e4d93cc3b4daProduct name920250630
62986c8d-91f1-b1ba-b5a3-8b54b75bb8c2Product name620250516
2194a6ab-15bb-de49-cced-f09e642b1b64Product name820240313
e42f429b-c4e5-0402-e1c5-730154df4060Product name420240205
38d4de13-64b3-4057-b91c-4b5126962341Product name120220516
089e0644-1ea8-8654-4113-39f960dd57d5Product name320210115
1629e00f-54fb-4a43-8306-b58442b23902Product name920200430
5331c9c8-f64b-11e6-ccf1-071c477fcb0bProduct name720190612
9f64e0dc-109c-9660-8e0e-91ec987b3817Product name620171204
dfa879a3-32de-49f0-a7ba-9b9c3e13002fProduct name120171204
8de20f81-8411-4cf1-a8b2-03404ee56d01Product name320171109
a5f1a68c-0352-4f34-46a3-9b4eed239ed8Product name220160819
d7840f4c-f22a-4403-b5da-53ac6ac8fd90Product name120150728
ccc7bb05-654a-45d2-a0d6-09ab96ba531bProduct name220150611
355b2224-0895-7135-83f5-d099a6a82a0aProduct name120140508
55be6b50-8cc0-f0f1-74a1-3416a91193aaProduct name120140508
7a0092d1-1e8c-0d78-4f8d-d95fa15cc3cfProduct name120140508
89b93c13-4be8-69f3-b33b-63e64feffb9bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71384-510-012022-01-28C16284748780-19d75b9d0-ecd1-f424-e053-dadaa90a57ce62fce8cd-0956-2830-e053-2991aa0a041c
71384-510-012020-02-10C16284748780-19d75b9d0-ecd1-f424-e053-dadaa90a57ce62fce8cd-0956-2830-e053-2991aa0a041c
71384-510-012020-01-31C16284748780-19d75b9d0-ecd1-f424-e053-dadaa90a57ce62fce8cd-0956-2830-e053-2991aa0a041c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71384-510-01Triamcinolone-Moxifloxacin PF20 in 1 BOXINJECTION, SUSPENSION204
71384-510-01Triamcinolone-Moxifloxacin PF0.6 mL in 1 VIAL, SINGLE-USEINJECTION, SUSPENSION0.64

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71384-510TRIAMCINOLONE-MOXIFLOXACIN PF INJECTION, SUSPENSION [IMPRIMIS NJOF, LLC]4Legacy NDC, 2 package rows20200211_62fce8cd-0956-2830-e053-2991aa0a041c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71384-510-01ML - Milliliter71384-510c3d8203d-e650-4fb6-b72a-f36ea86d269112018-07-03

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71384-51071384-510-01

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
NameUNIIKind
TRIAMCINOLONE ACETONIDEF446C597KAACTIB
MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATEB8956S8609ACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
9e3e5211-e5c5-1dd8-e053-2995a90a961d62fce8cd-0956-2830-e053-2991aa0a041c2020-02-10Exact identifier
spl id: 9e3e5211-e5c5-1dd8-e053-2995a90a961d
spl set id: 62fce8cd-0956-2830-e053-2991aa0a041c

Reported adverse events (FAERS/openFDA)#

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