Ixiaro Injection, Suspension
NDC Package 62195-051-01
Package Information
Ixiaro (japanese encephalitis vaccine, inactivated, adsorbed) injection is classified as a
- actively acquired immunity - [pe] (physiologic effect)
- inactivated japanese encephalitis virus vaccine - [epc] (established pharmacologic class)
- japanese encephalitis vaccines - [cs]
- vaccines administered via intramuscular route. This formulation utilizes a injection, suspension delivery system. Marketed by Vetter Pharma Fertigung Gmbh & Co. Kg, this product is identified by NDC 62195-051 and is authorized under FDA application BLA125280.
Identification & Billing
- RxCUI: 1300781 - Japanese encephalitis vaccine 6 MCG in 0.5 ML Prefilled Syringe
- RxCUI: 1300781 - 0.5 ML Japanese encephalitis virus vaccine Nakayama-NIH strain, inactivated 0.012 MG/ML Prefilled Syringe
- RxCUI: 1300781 - Japanese encephalitis virus vaccine Nakayama-NIH strain, inactivated 6 MCG per 0.5 ML Prefilled Syringe
- RxCUI: 1300783 - IXIARO 6 MCG in 0.5 ML Prefilled Syringe
- RxCUI: 1300783 - 0.5 ML Japanese encephalitis virus vaccine Nakayama-NIH strain, inactivated 0.012 MG/ML Prefilled Syringe [Ixiaro]
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 62195 - Vetter Pharma Fertigung Gmbh & Co. Kg
- 62195-051 - Ixiaro
- 62195-051-01 - .5 mL in 1 SYRINGE
- 62195-051 - Ixiaro
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 62195-051-01 identifies a specific commercial package of .5 ml in 1 syringe of Ixiaro, a vaccine label labeled by Vetter Pharma Fertigung Gmbh & Co. Kg. This injection, suspension is formulated for intramuscular use and contains japanese encephalitis virus strain sa 14-14-2 antigen (formaldehyde inactivated) as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Vetter Pharma Fertigung Gmbh & Co. Kg on March 30, 2009. The current certification is valid through December 31, 2026.
How is this Vetter Pharma Fertigung Gmbh & Co. Kg product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 62195005101. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.