NDC 63776-175 Viatrexx-f Gus

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63776-175
Proprietary Name:
Viatrexx-f Gus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Viatrexx Bio Incorporated
Labeler Code:
63776
Start Marketing Date: [9]
03-29-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 63776-175-11

Package Description: .5 mL in 1 AMPULE

NDC Code 63776-175-14

Package Description: 30 mL in 1 BOTTLE

NDC Code 63776-175-15

Package Description: 50 mL in 1 BOTTLE

NDC Code 63776-175-16

Package Description: 100 mL in 1 BOTTLE

NDC Code 63776-175-17

Package Description: 250 mL in 1 BOTTLE

NDC Code 63776-175-18

Package Description: 500 mL in 1 BOTTLE

NDC Code 63776-175-19

Package Description: 1000 mL in 1 BOTTLE

Product Details

What is NDC 63776-175?

The NDC code 63776-175 is assigned by the FDA to the product Viatrexx-f Gus which is product labeled by Viatrexx Bio Incorporated. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 63776-175-11 .5 ml in 1 ampule , 63776-175-14 30 ml in 1 bottle , 63776-175-15 50 ml in 1 bottle , 63776-175-16 100 ml in 1 bottle , 63776-175-17 250 ml in 1 bottle , 63776-175-18 500 ml in 1 bottle , 63776-175-19 1000 ml in 1 bottle . 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.

What are the uses for Viatrexx-f Gus?

Nutritional support for fungal, mold, bacteria challenges 

Which are Viatrexx-f Gus UNII Codes?

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

Which are Viatrexx-f Gus 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:

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Product Footnotes

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

[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".