Jynneos Injection, Suspension
NDC 50632-022
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
Jynneos (vaccinia virus modified strain ankara-bavarian nordic non-replicating antigen) is a BLA-approved product labeled by Bavarian Nordic A/s. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a injection, suspension for subcutaneous administration. This product entry covers the primary NDC 50632-022 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
50632-022
Proprietary Name:
Jynneos
Non-Proprietary Name: [1]
Vaccinia Virus Modified Strain Ankara-bavarian Nordic Non-replicating Antigen
Substance Name: [2]
Vaccinia Virus Modified Strain Ankara-bavarian Nordic Non-replicating Antigen
NDC Directory Status:
Vaccine
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
Dosage Form:
Injection, Suspension
- A liquid preparation, suitable for injection, which consists of solid particles dispersed throughout a liquid phase in which the particles are not soluble. It can also consist of an oil phase dispersed throughout an aqueous phase, or vice-versa.
Administration Route(s): [4]
Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
50632
Product Label ID:
FDA Application Number: [6]
BLA125678
Marketing Category: [8]
BLA - A product marketed under an approved Biologic License Application.
Marketing Timeline
Start Marketing Date: [9]
02-14-2025
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 50632-022?
The NDC code 50632-022 is assigned by the FDA to the product Jynneos. It is commonly known by its generic name, vaccinia virus modified strain ankara-bavarian nordic non-replicating antigen. This pharmaceutical product is labeled by Bavarian Nordic A/s and is currently categorized as listed product. The medication is a injection, suspension administered via subcutaneous route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 50632-022-02. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
JYNNEOS is a vaccine indicated for prevention of smallpox and mpox disease in adults 18 years of age and older determined to be at high risk for smallpox or mpox infection.
What are Active Ingredients of this product?
An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- VACCINIA VIRUS MODIFIED STRAIN ANKARA-BAVARIAN NORDIC NON-REPLICATING ANTIGEN (UNII: TU8J357395)
- VACCINIA VIRUS MODIFIED STRAIN ANKARA-BAVARIAN NORDIC NON-REPLICATING ANTIGEN (UNII: TU8J357395) (Active Moiety)
Which are the Inactive Ingredients associated UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- TROMETHAMINE (UNII: 023C2WHX2V)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for this product?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
- RxCUI: 2464827 - smallpox and monkeypox vaccine, live 0.5 mL Injection
- RxCUI: 2464827 - 0.5 ML modified Vaccinia Ankara-Bavarian Nordic 198000000 UNT/ML Injection
- RxCUI: 2464827 - modified Vaccinia Ankara-Bavarian Nordic 198000000 UNT/ML per 0.5 MLInjection
- RxCUI: 2464827 - modified Vaccinia Ankara-Bavarian Nordic 395000000 UNT per 1 ML Injection
- RxCUI: 2464827 - MVA-BN 198000000 UNT/ML per 0.5 MLInjection
* Please review the full disclaimer at the bottom of this page.
Patient Education
Smallpox/Mpox Vaccine
Why get vaccinated? Smallpox/Mpox vaccine can prevent infection with some types of orthopoxviruses including Smallpox, Mpox, and Vaccinia viruses. Smallpox infection can cause a serious illness characterized by rash and fever that may result in death, for some. Mpox infection can cause an illness similar to Smallpox. Although generally milder, it can still cause death. Vaccinia virus infection can occur after someone is exposed to a person or an animal who has been exposed to the virus. It generally causes a self-limiting illness.
[Learn More]
* Please review the full disclaimer at the bottom of this page.
Product & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What is the Substance Name? An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
What kind of product is this? Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the FDA Application Number? This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
What is the NDC Exclude Flag? This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
