The NDC Code 50090-1493-0 is assigned to a package of 1 syringe in 1 pouch > .5 ml in 1 syringe of Typhim Vi, a vaccine lable labeled by A-s Medication Solutions. The product's dosage form is injection, solution and is administered via intramuscular form.
||1 SYRINGE in 1 POUCH > .5 mL in 1 SYRINGE
||Typhim Vi What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
||Salmonella Typhi Ty2 Vi Polysaccharide Antigen 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.
||This vaccine is used to help prevent typhoid fever. Vaccines work by increasing the body's natural defense (immunity) against the bacteria that cause the infection. This vaccine is recommended for people who are traveling to areas where the infection is common (e.g., Africa, Asia, Central/South America), those who are in close contact to someone with persistent typhoid infection, and those who work with the bacteria (Salmonella typhi) in a laboratory. This vaccine is used to prevent the disease and will not treat typhoid fever or a persistent typhoid infection.
|11-Digit NDC Billing Format
||50090149300 NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
||ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
||Vaccine 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.
A-s Medication Solutions
||Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
- Intramuscular - Administration within a muscle.
- SALMONELLA TYPHI TY2 VI POLYSACCHARIDE ANTIGEN 25 ug/.5mL
- Inactivated Salmonella Typhi Vaccine - [EPC] (Established Pharmacologic Class)
- Actively Acquired Immunity - [PE] (Physiologic Effect)
- Vaccines -
- Inactivated - [CS]
- Vaccines -
- Typhoid - [CS]
- Polysaccharides -
- Bacterial - [CS]
||No Sample Package?
This field Indicates whether this package is a sample packaging or not.
||BLA - A product marketed under an approved Biologic License Application. 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.
|FDA Application Number
||BLA103936 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.
|Start Marketing Date
||11-28-1994 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
|Listing Expiration Date
||12-31-2022 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.
||N 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".
NDC Code Structure
- 50090 - A-s Medication Solutions
- 50090-1493 - Typhim Vi
50090-1493-0 - 1 SYRINGE in 1 POUCH
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.
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