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  5. NDC Package Code: 69307-4496-2 Vanilla Silq Hd

NDC Package 69307-4496-2 Vanilla Silq Hd

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
69307-4496-2
Package Description:
310 g in 1 BOTTLE, PLASTIC
Product Code:
69307-4496
Proprietary Name:
Vanilla Silq Hd
Usage Information:
This product should not be used in patients with known or suspected gastric or intestinal perforation, patients with conditions that may increase the risk of perforation; hypersensitivity to barium sulfate products; suspected tracheoesophageal fistula; obstructing lesions of the small intestine; pyloric stenosis; inflammation or neoplastic lesions of the rectum; or in patients who have had a recent rectal biopsy.Barium sulfate suspensions should not be used for infants with swallowing disorders or for newborns with complete duodenal or jejunal obstruction or when distal small bowel or colon obstruction is suspected. Barium sulfate suspension is not recommended for very small preterm infants and young babies requiring small volumes of contrast media or for infants and young children when there is a possibility of leakage from the gastrointestinal tract, such as nectrotizing enterocolitis, unexplained pneumoperitoneum, gasless abdomen, other bowel perforation, esophageal perforation or post operative anastomosis.
11-Digit NDC Billing Format:
69307449602
Labeler Name:
Genus Medical Technologies, Llc
Sample Package:
No
Start Marketing Date:
12-08-2015
Listing Expiration Date:
12-31-2022
Exclude Flag:
I
Code Structure:

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.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 69307-4496-2?

The NDC Packaged Code 69307-4496-2 is assigned to a package of 310 g in 1 bottle, plastic of Vanilla Silq Hd, labeled by Genus Medical Technologies, Llc. The product's dosage form is and is administered via form.

Is NDC 69307-4496 included in the NDC Directory?

No, Vanilla Silq Hd with product code 69307-4496 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Genus Medical Technologies, Llc on December 08, 2015 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 69307-4496-2?

The 11-digit format is 69307449602. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-169307-4496-25-4-269307-4496-02