Vivotif Capsule, Coated
Product Images NDC 50632-016

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Vivotif (NDC 50632-016). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bavarian Nordic A/s, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Rx Only (Image 01)

Vivotif capsule packaging label featuring the vaccine Salmonella typhi Ty21a, with a strength of 6 billion CFU per capsule. The product is labeled for oral administration. The label shows the Bavarian Nordic A/S as the manufacturer and includes the product NDC 50632-016. The packaging indicates it is a coated capsule vaccine.*

FDA Label Image

Typhoid Vaccine Live Oral Ty21a Vivotif Carton Label (Image 02)

Packaging label for Vivotif Typhoid Vaccine Live Oral Ty21a, an oral coated capsule vaccine containing live attenuated Salmonella typhi strain Ty21a. The label includes dosing information, storage instructions to refrigerate, the NDC number 50632-016-02, and manufacturer Bavarian Nordic A/S from Denmark. Barcode and lot/expiration date fields are also present.*

FDA Label Image

Typhoid Vaccine Live Oral Ty21a Vivotif Blister Label (Image 03)

The image shows four identical medication labels for Vivotif, a Typhoid Vaccine Live Oral Ty21a capsule. Each label states the vaccine is oral, live, and each capsule contains 2.0-10 x 10^9 CFU. The labeler is Bavarian Nordic A/S, Denmark, with US license number 2096 and NDC 50632-016-04. The labels feature barcodes and Rx-only designation.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.