NDC 69307-1024 Vanilla Silq

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:
69307-1024
Proprietary Name:
Vanilla Silq
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Genus Medical Technologies, Llc
Labeler Code:
69307
Start Marketing Date: [9]
10-27-2014
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69307-1024-2

Package Description: 450 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 69307-1024?

The NDC code 69307-1024 is assigned by the FDA to the product Vanilla Silq which is product labeled by Genus Medical Technologies, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69307-1024-2 450 ml in 1 bottle, plastic . 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 Vanilla Silq?

INDICATIONS AND USAGE: For use as a contrast agent in radiographic studies.

Which are Vanilla Silq UNII Codes?

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

* Please review the disclaimer below.

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".