Cyclosporine/Chondroitin Sulfate PF

Manufacturer
ImprimisRx NJ
Effective date
2018-02-26
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:25:26

Label at a glance#

ProductCyclosporine/Chondroitin Sulfate PF
Active ingredientCYCLOSPORINE
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.PRINCIPAL DISPLAY PANEL

Bottle LabelBottle Label

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CYCLOSPORINE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
1be408a0-e15a-4092-b35e-4e294e65196fProduct name320240216
b3fdee3e-0c46-442f-aad5-aa71941d5621Product name120231023
78fb0708-fce5-decd-6611-5a9fbe3e3decProduct name320230327
54840517-000d-4fcb-b976-a6ddd102faa0Product name120220120
a5ba3bd0-8411-4005-ac3b-a41d8ee0633aProduct name120181029
b1c0d609-8b97-06ee-2cd0-5652a4b1d019Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70261-514-052020-01-31C16284748780-19d75b9d0-3d78-f424-e053-dadaa90a57ce6623a4de-d95c-7aef-e053-2991aa0a9235

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70261-514-05Cyclosporine/Chondroitin Sulfate PF5.5 mL in 1 BOTTLE, DROPPEREMULSION5.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70261-514CYCLOSPORINE/CHONDROITIN SULFATE PF EMULSION [IMPRIMISRX NJ]1Legacy NDC, 1 package rows20180227_6623a4de-d95c-7aef-e053-2991aa0a9235.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70261-51470261-514-05

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
NameUNIIKind
CYCLOSPORINE83HN0GTJ6DACTIB

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
6623a4de-d95d-7aef-e053-2991aa0a92356623a4de-d95c-7aef-e053-2991aa0a92352018-02-26Exact identifier
spl id: 6623a4de-d95d-7aef-e053-2991aa0a9235
spl set id: 6623a4de-d95c-7aef-e053-2991aa0a9235

Reported adverse events (FAERS/openFDA)#

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