NDC 17478-609-01 - ZIOPTAN

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 17478-609
Requested NDC: 17478-609-01
Package NDCs from labels: 17478-609-01, 17478-609-90, 17478-609-30, 17478-609-10
Manufacturer: Akorn
Effective date: 2022-10-04
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
ZIOPTAN - Akorn	Akorn	2022-10-04	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
17478-609-10	2024-01-30	C162847	48780-1	1030e365-287f-111a-e063-dadaa90a10e2	These highlights do not include all the information needed to use ZIOPTAN ® (tafluprost ophthalmic solution) 0.0015% safely and effectively. See full prescribing information for ZIOPTAN ® . ZIOPTAN ® (tafluprost ophthalmic solution) 0.0015% Initial U.S. Approval: 2012
17478-609-30	2024-01-30	C162847	48780-1	1030e365-287f-111a-e063-dadaa90a10e2	These highlights do not include all the information needed to use ZIOPTAN ® (tafluprost ophthalmic solution) 0.0015% safely and effectively. See full prescribing information for ZIOPTAN ® . ZIOPTAN ® (tafluprost ophthalmic solution) 0.0015% Initial U.S. Approval: 2012
17478-609-90	2024-01-30	C162847	48780-1	1030e365-287f-111a-e063-dadaa90a10e2	These highlights do not include all the information needed to use ZIOPTAN ® (tafluprost ophthalmic solution) 0.0015% safely and effectively. See full prescribing information for ZIOPTAN ® . ZIOPTAN ® (tafluprost ophthalmic solution) 0.0015% Initial U.S. Approval: 2012

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
17478-609-01	ZIOPTAN	10 in 1 POUCH	SOLUTION/ DROPS	10	10
17478-609-01	ZIOPTAN	0.3 mL in 1 VIAL, SINGLE-USE	SOLUTION/ DROPS	0.3	10
17478-609-10	ZIOPTAN	1 in 1 CARTON	SOLUTION/ DROPS	1	10
17478-609-30	ZIOPTAN	3 in 1 CARTON	SOLUTION/ DROPS	3	10
17478-609-90	ZIOPTAN	9 in 1 CARTON	SOLUTION/ DROPS	9	10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
17478-609	ZIOPTAN (TAFLUPROST) SOLUTION/ DROPS [AKORN]	10	Legacy NDC, 5 package rows	20221005_a3173c26-0e19-47af-a01c-3fc06b2700d1.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
17478-609-01	EA - Each	17478-609	08d454dd-4bac-4f88-ae52-b1535c54ce1f	1	2015-07-20
17478-609-30	EA - Each	17478-609	90cf9725-5826-47c8-91f9-0d75126df853	1	2015-01-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Tafluprost	ACTIVE INGREDIENT	1O6WQ6T7G3	ZIOPTAN (TAFLUPROST) SOLUTION/ DROPS [AKORN, INC.]	2
Tafluprost	ACTIVE MOIETY	1O6WQ6T7G3	ZIOPTAN (TAFLUPROST) SOLUTION/ DROPS [AKORN, INC.]	2
Edetate Disodium	INACTIVE INGREDIENT	7FLD91C86K	ZIOPTAN (TAFLUPROST) SOLUTION/ DROPS [AKORN, INC.]	2
Glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	ZIOPTAN (TAFLUPROST) SOLUTION/ DROPS [AKORN, INC.]	2
Hydrochloric Acid	INACTIVE INGREDIENT	QTT17582CB	ZIOPTAN (TAFLUPROST) SOLUTION/ DROPS [AKORN, INC.]	2
Polysorbate 80	INACTIVE INGREDIENT	6OZP39ZG8H	ZIOPTAN (TAFLUPROST) SOLUTION/ DROPS [AKORN, INC.]	2
Sodium Hydroxide	INACTIVE INGREDIENT	55X04QC32I	ZIOPTAN (TAFLUPROST) SOLUTION/ DROPS [AKORN, INC.]	2
Sodium Phosphate, Monobasic, Dihydrate	INACTIVE INGREDIENT	5QWK665956	ZIOPTAN (TAFLUPROST) SOLUTION/ DROPS [AKORN, INC.]	2
Water	INACTIVE INGREDIENT	059QF0KO0R	ZIOPTAN (TAFLUPROST) SOLUTION/ DROPS [AKORN, INC.]	2

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 8 of 25 · 491 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
GoodSense Redness Relief Plus	GLLYCERIN, NAPHAZOLINE HYDROCHLORIDE	Geiss, Destin & Dunn, Inc.	9b37250f-9bdf-574e-e053-2a95a90a013e	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
CVS Maximum Redness Relief	GLYCERIN, NAPHAZOLINE HCI	CVS Pharmacy, Inc.	f70f9fc4-4022-336e-e053-6394a90a4d07	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
Discount Drug Mart Eye Drops Dry Eye Relief	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	Discount Drug Mart	f7fd53be-e501-d97f-e053-6394a90ad409	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
Family Wellness Maximum Redness Relief Eye Drops	GLYCERIN, NAPHAZOLINE HCL	Family Dollar Services, Inc.	facd53c4-9cfc-6589-e053-6394a90a180d	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
Exchange Select Artificial Tears Lubricant Eye Drops	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	Army and Air Force Exchange Service	9e478343-8ae7-823e-e053-2995a90a84ed	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
Medics Choice Eye Drops Maximum Redness Relief	GLYCERIN, NAPHAZOLINE HYDROCHLORIDE	K.C. Pharmaceuticals, Inc.	f7131707-47af-d70a-e053-6394a90a418f	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
DG Health Dry Eye Relief	GLYCERIN, HYPROMELLOSE, POLYPROPYLENE GLYCOL 400	Dolgencorp LLC	9cb20c3b-bf6d-8c7c-e053-2995a90aa485	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
DG Maximum Strength Redness Relief	GLYCERIN, NAPHAZOLINE HCL	Dolgencorp, Inc	9cb261ed-b708-1189-e053-2a95a90a547d	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
Winco Maximum Redness Relief Eye Drops	GLYCERIN, NAPHAZOLINE HCL	WinCo Foods, LLC	ff3651d4-42ce-4db1-a318-15f7592baf86	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
Core Values Eye Drops Dry Eye Relief	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	Liberty Procurement Co. Inc.	f8285f68-c40c-19a8-e053-6394a90aacad	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
Harris Teeter Eye Drops Artificial Tears	GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	Harris Teeter, LLC.	f82957d9-c4ad-a914-e053-6294a90aac50	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
Harris Teeter Eye Drops Maximum Redness Relief	GLYCERIN, NAPHAZOLINE HYDROCHLORIDE	Harris Teeter, LLC	f710d107-0403-21c5-e053-6394a90a0372	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
Foster and Thrive Redness Relief Eye Drops	GLYCERIN, NAPHAZOLINE HCL	Strategic Sourcing Services LLC	0042e9a0-9693-d7e0-e063-6294a90ae6c6	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
CareOne Maximum Redness Relief Eye Drops	GLYCERIN, NAPHAZOLINE HCI	Retail Business Services, LLC	9ab96aed-21d3-11b6-e053-2995a90a7225	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
Equate Redness and Dry Eye Relief Eye Drops	GLYCERIN, NAPHAZOLINE HCL	Wal-Mart Stores, Inc.	ae228018-9238-2cbd-e053-2995a90a8d99	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
Eye Love Heyedrate Long Lasting Hydration	GLYCERIN, POVIDONE	Physician Recommended Neutraceuticals, L.P.	f321dea1-3251-eaa8-e053-2995a90aaf95	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
Quality Choice Eye Wash	WATER	Chain Drug Marketing Assoc., Inc.	1fb8a109-351b-7039-e063-6394a90a7311	2025-12-30	Warnings	Exact identifier unii: 059QF0KO0R
Rite Aid Eye Wash	PURIFIED WATER	Rite Aid	28a18e04-d735-a511-e063-6394a90af6bb	2025-12-30	Warnings	Exact identifier unii: 059QF0KO0R
Equate Optimal Hydration Lubricant Eye Drops	CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN	Walmart, Inc.	151b9723-5d5e-ac2b-e063-6294a90af073	2025-12-30	Warnings	Exact identifier unii: PDC6A3C0OX
OCUFRESH	WATER	Optics Laboratory Inc.	b8e477a9-66b9-496b-92fb-3d4bbd7b36b5	2025-12-29	Warnings	Exact identifier unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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