Hgh Plus Liquid
NDC Package 55856-0003-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
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.

Hgh Plus (adrenalinum, thyroidinum (suis), insulinum, pituitaria glandula (suis),) liquids is classified as a

administered via oral route. This formulation utilizes a liquid delivery system. Marketed by Life Choice Ltd., this product is identified by NDC 55856-0003.

Identification & Billing

NDC Package Code
55856-0003-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
55856-0003
11-Digit Billing Format
55856000301

Clinical Specifications

Proprietary Name
Hgh Plus
Non-Proprietary Name
Adrenalinum, Thyroidinum (suis), Insulinum, Pituitaria Glandula (suis),
Substance Name
Epinephrine; Insulin Human; Sus Scrofa Pituitary Gland, Posterior; Thyroid
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class

Regulatory & Marketing

Labeler Name
Life Choice Ltd.
Product Type
Human Prescription Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
03-10-2014
End Marketing Date
07-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 55856-0003-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Hgh Plus, a human prescription drug labeled by Life Choice Ltd.. This liquid is formulated for oral use and contains epinephrine; insulin human; sus scrofa pituitary gland, posterior; thyroid as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Life Choice Ltd. on March 10, 2014.

How is this Life Choice Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55856000301. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
55856-0003-1
11-Digit CMS (5-4-2)
55856-0003-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.