1. Home
  2. Labeler Index
  3. Ratis, Llc
  4. 71753-1152
  5. NDC Package Code: 71753-1152-1 Thymuline

NDC Package 71753-1152-1 Thymuline

Liquid Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

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:
71753-1152-1
Package Description:
30 mL in 1 BOTTLE, SPRAY
Product Code:
71753-1152
Proprietary Name:
Thymuline
Non-Proprietary Name:
Thymuline
Substance Name:
Nonathymulin
Usage Information:
Immune system support.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration. Immune system support.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
11-Digit NDC Billing Format:
71753115201
Product Type:
Human Otc Drug
Labeler Name:
Ratis, Llc
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
NONATHYMULIN 9 [hp_C]/mL
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
09-06-2018
End Marketing Date:
12-01-2025
Exclude Flag:
N
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 71753-1152-1?

The NDC Packaged Code 71753-1152-1 is assigned to a package of 30 ml in 1 bottle, spray of Thymuline, a human over the counter drug labeled by Ratis, Llc. The product's dosage form is liquid and is administered via oral form.

Is NDC 71753-1152 included in the NDC Directory?

Yes, Thymuline with product code 71753-1152 is active and included in the NDC Directory. The product was first marketed by Ratis, Llc on September 06, 2018.

What is the 11-digit format for NDC 71753-1152-1?

The 11-digit format is 71753115201. 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
5-4-171753-1152-15-4-271753-1152-01