Cyclosporine/Chondroitin PF

Manufacturer: Imprimis NJOF, LLC
Effective date: 2020-02-10
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 20:32:16

Label at a glance#

ProductCyclosporine/Chondroitin 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 Label

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
CYCLOSPORINE Pharmacologic Class Indexing	3	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
1be408a0-e15a-4092-b35e-4e294e65196f	Product name	3	20240216
b3fdee3e-0c46-442f-aad5-aa71941d5621	Product name	1	20231023
78fb0708-fce5-decd-6611-5a9fbe3e3dec	Product name	3	20230327
54840517-000d-4fcb-b976-a6ddd102faa0	Product name	1	20220120
a5ba3bd0-8411-4005-ac3b-a41d8ee0633a	Product name	1	20181029
b1c0d609-8b97-06ee-2cd0-5652a4b1d019	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71384-514-05	2022-01-28	C162847	48780-1	9d75b9d0-d597-f424-e053-dadaa90a57ce	6ef02195-0ad6-0c27-e053-2991aa0aecb2
71384-514-05	2020-02-10	C162847	48780-1	9d75b9d0-d597-f424-e053-dadaa90a57ce	6ef02195-0ad6-0c27-e053-2991aa0aecb2
71384-514-05	2020-01-31	C162847	48780-1	9d75b9d0-d597-f424-e053-dadaa90a57ce	6ef02195-0ad6-0c27-e053-2991aa0aecb2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71384-514-05	Cyclosporine/Chondroitin PF	5.5 mL in 1 BOTTLE, DROPPER	EMULSION	5.5		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71384-514	CYCLOSPORINE/CHONDROITIN PF (CYCLOSPORINE/CHONDROITIN SULFATE PF) EMULSION [IMPRIMIS NJOF, LLC]	2	Legacy NDC, 1 package rows	20200211_6ef02195-0ad6-0c27-e053-2991aa0aecb2.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
71384-514-05	ML - Milliliter	71384-514	398683af-eb3e-4e89-ae37-32501c41d80f	1	2018-07-03

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Cyclosporine/Chondroitin PF
Cyclosporine/Chondroitin Sulfate PF
CYCLOSPORINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71384-514	71384-514-05

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
Name	UNII	Kind
CYCLOSPORINE	83HN0GTJ6D	ACTIB

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
9e3fb384-3c93-a772-e053-2a95a90a6eba			6ef02195-0ad6-0c27-e053-2991aa0aecb2	2020-02-10		Exact identifier spl id: 9e3fb384-3c93-a772-e053-2a95a90a6eba spl set id: 6ef02195-0ad6-0c27-e053-2991aa0aecb2

Reported adverse events (FAERS/openFDA)#

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