NDC 17478-609

ZIOPTAN

Tafluprost

ZIOPTAN is a Ophthalmic Solution/ Drops in the Human Prescription Drug category. It is labeled and distributed by Akorn, Inc.. The primary component is Tafluprost.

• Product ID: 17478-609_01a2a304-9308-44dd-9c0f-db4d24757f5b
• NDC: 17478-609
• Product Type: Human Prescription Drug
• Proprietary Name: ZIOPTAN
• Generic Name: Tafluprost
• Dosage Form: Solution/ Drops
• Route of Administration: OPHTHALMIC
• Marketing Start Date: 2014-11-26
• Marketing Category: NDA / NDA
• Application Number: NDA202514
• Labeler Name: Akorn, Inc.
• Substance Name: TAFLUPROST
• Active Ingredient Strength: 0 mg/.3mL
• Pharm Classes: Prostaglandin Analog [EPC],Prostaglandin Receptor Agonists [MoA],Increased Prostaglandin Activity [PE],Prostaglandins [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 17478-609-10

1 POUCH in 1 CARTON (17478-609-10) > 10 VIAL, SINGLE-USE in 1 POUCH (17478-609-01) > .3 mL in 1 VIAL, SINGLE-USE

• Marketing Start Date: 2017-11-26
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17478-609-90 [17478060990]

ZIOPTAN SOLUTION/ DROPS

• Marketing Category: NDA
• Application Number: NDA202514
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-11-26

NDC 17478-609-10 [17478060910]

ZIOPTAN SOLUTION/ DROPS

• Marketing Category: NDA
• Application Number: NDA202514
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-11-26

NDC 17478-609-01 [17478060901]

ZIOPTAN SOLUTION/ DROPS

• Marketing Category: NDA
• Application Number: NDA202514
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2014-11-26

NDC 17478-609-30 [17478060930]

ZIOPTAN SOLUTION/ DROPS

• Marketing Category: NDA
• Application Number: NDA202514
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2017-11-26

Drug Details

Active Ingredients

Ingredient	Strength
TAFLUPROST	.0045 mg/.3mL

OpenFDA Data

• SPL SET ID: a3173c26-0e19-47af-a01c-3fc06b2700d1
• Manufacturer:
  • Akorn, Inc.
• UNII:
  • 1O6WQ6T7G3
• RxNorm Concept Unique ID - RxCUI:
  • 1244616
  • 1244611
• UPC Code:
  • 0317478609018
  • 0317478609308

Pharmacological Class

• Prostaglandin Analog [EPC]
• Prostaglandin Receptor Agonists [MoA]
• Increased Prostaglandin Activity [PE]
• Prostaglandins [CS]

Medicade Reported Pricing

17478060930 ZIOPTAN 0.0015% EYE DROPS

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "ZIOPTAN" or generic name "Tafluprost"

NDC	Brand Name	Generic Name
17478-609	ZIOPTAN	tafluprost
82584-609	ZIOPTAN	Tafluprost
0781-6184	Tafluprost	Tafluprost
65302-062	Tafluprost	Tafluprost
66993-429	Tafluprost Ophthalmic	tafluprost