NDC 49281-790 Typhim Vi
Salmonella Typhi Ty2 Vi Polysaccharide Antigen Injection, Solution Intramuscular - View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 49281-790?
What are the uses for Typhim Vi?
What are Typhim Vi Active Ingredients?
Which are Typhim Vi UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALMONELLA TYPHI TY2 VI POLYSACCHARIDE ANTIGEN (UNII: 7194H8W3KT)
- SALMONELLA TYPHI TY2 VI POLYSACCHARIDE ANTIGEN (UNII: 7194H8W3KT) (Active Moiety)
Which are Typhim Vi 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: 94255I6E2T)
- SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)
- PHENOL (UNII: 339NCG44TV)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Typhim Vi?
- RxCUI: 1486496 - Typhim Vi 0.5 ML Prefilled Syringe
- RxCUI: 1486496 - 0.5 ML typhoid Vi polysaccharide vaccine, S typhi Ty2 strain 0.05 MG/ML Prefilled Syringe [Typhim VI]
- RxCUI: 1486496 - 0.5 ML Typhim VI 0.05 MG/ML Prefilled Syringe
- RxCUI: 1486496 - Typhim VI 25 MCG per 0.5 ML Prefilled Syringe
- RxCUI: 807222 - typhoid Vi polysaccharide vaccine (generic for Typhim Vi) Injectable Solution
Which are the Pharmacologic Classes for Typhim Vi?
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Patient Education
Typhoid Vaccine
What is typhoid? Typhoid (typhoid fever) is a serious disease. It is caused by bacteria called Salmonella Typhi. Typhoid causes a high fever, fatigue, weakness, stomach pains, headache, loss of appetite, and sometimes a rash. If it is not treated, it can kill up to 30% of people who get it. Some people who get typhoid become ''carriers,'' who can spread the disease to others. Generally, people get typhoid from contaminated food or water. Typhoid is rare in the U.S., and most U.S. citizens who get the disease get it while traveling. Typhoid strikes about 21 million people a year around the world and kills about 200,000.
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[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.
[2] 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.
[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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] 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.
[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".