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NDC 49281-913 Stamaril

Yellow Fever Virus Strain 17d-204 Live Antigen Kit - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 49281-913?
  4. Active Ingredients UNII Codes
  5. Inactive Ingredients UNII Codes
  6. NDC to RxNorm Crosswalk
  7. Patient Education

Product Information

NDC Product Code:
49281-913
Proprietary Name:
Stamaril
Non-Proprietary Name: [1]
Yellow Fever Virus Strain 17d-204 Live Antigen
NDC Directory Status:
Vaccine
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Sanofi Pasteur Inc.
Labeler Code:
49281
Product Label ID:
b557ec63-3599-4372-b4f8-ea022b4e3712
Marketing Category: [8]
UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE -
Start Marketing Date: [9]
09-27-2016
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
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Product Details

What is NDC 49281-913?

The NDC code 49281-913 is assigned by the FDA to the product Stamaril which is a vaccine label product labeled by Sanofi Pasteur Inc.. The generic name of Stamaril is yellow fever virus strain 17d-204 live antigen. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 49281-913-01 1 kit in 1 carton * .5 ml in 1 vial, single-use * .5 ml in 1 syringe (49281-911-58). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

Which are Stamaril UNII Codes?

The UNII codes for the active ingredients in this product are:

  • YELLOW FEVER VIRUS STRAIN 17D-204 LIVE ANTIGEN (UNII: PY4EET359T)
  • YELLOW FEVER VIRUS STRAIN 17D-204 LIVE ANTIGEN (UNII: PY4EET359T) (Active Moiety)

Which are Stamaril Inactive Ingredients 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:

What is the NDC to RxNorm Crosswalk for Stamaril?

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: 1876705 - yellow fever vaccine (generic for Stamaril) 0.5 ML Injection
  • RxCUI: 1876705 - 0.5 ML yellow fever virus strain 17D-204 live antigen 2000 UNT/ML Injection
  • RxCUI: 1876710 - STAMARIL 0.5 ML Injection
  • RxCUI: 1876710 - 0.5 ML yellow fever virus strain 17D-204 live antigen 2000 UNT/ML Injection [Stamaril]
  • RxCUI: 1876710 - 0.5 ML Stamaril 2000 UNT/ML Injection

* Please review the disclaimer below.

Patient Education

Yellow Fever Vaccine


What is yellow fever? Yellow fever is a serious disease caused by the yellow fever virus. It is found in certain parts of Africa and South America. Yellow fever is spread through the bite of an infected mosquito. It cannot be spread person to person by direct contact. People with yellow fever disease usually have to be hospitalized. Yellow fever can cause: fever and flu-like symptoms jaundice (yellow skin or eyes) bleeding from multiple body sites liver, kidney, respiratory and other organ failure death (20 to 50% of serious cases) Yellow fever vaccine is a live, weakened virus. It is given as a single shot. For people who remain at risk, a booster dose is recommended every 10 years. Yellow fever vaccine may be given at the same time as most other vaccines.
[Learn More]


* Please review the disclaimer below.

Product Footnotes

[1] 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.

[3] 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.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".