1. Home
  2. Labeler Index
  3. Medinatura
  4. 50114-8200
  5. NDC Package Code: 50114-8200-3 Lymphomyosot X

NDC Package 50114-8200-3 Lymphomyosot X

Araneus Diadematus,Tribasic Calcium Phosphate,Equisetum Hyemale,Ferrous Iodide, Fumaria - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

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:
50114-8200-3
Package Description:
3 AMPULE in 1 CARTON / 1.1 mL in 1 AMPULE
Product Code:
50114-8200
Proprietary Name:
Lymphomyosot X
Non-Proprietary Name:
Araneus Diadematus, Tribasic Calcium Phosphate, Equisetum Hyemale, Ferrous Iodide, Fumaria Officinalis Flowering Top, Gentiana Lutea Root, Geranium Robertianum, Myosotis Arvensis, Nasturtium Officinale, Sodium Sulfate, Pinus Sylvestris Leafy Twig, Smilax Regelii Root, Scrophularia Nodosa, Teucrium Scorodonia Flowering Top, Thyroid, Unspecified Andveronica Officinalis Flowering Top
Substance Name:
Araneus Diadematus; Equisetum Hyemale; Ferrous Iodide; Fumaria Officinalis Flowering Top; Gentiana Lutea Root; Geranium Robertianum; Myosotis Arvensis; Nasturtium Officinale; Pinus Sylvestris Leafy Twig; Scrophularia Nodosa; Smilax Ornata Root; Sodium Sulfate; Teucrium Scorodonia Flowering Top; Thyroid, Unspecified; Tribasic Calcium Phosphate; Veronica Officinalis Flowering Top
Usage Information:
Lymphomyosot® X Injection Solution is contraindicationed in patients with known hypersensiticety to Lymphomyost® X or any of its ingredients.
11-Digit NDC Billing Format:
50114820003
Product Type:
Human Prescription Drug
Labeler Name:
Medinatura
Dosage Form:
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route(s):
  • Intradermal - Administration within the dermis.
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
    • Active Ingredient(s):
  • ARANEUS DIADEMATUS 6 [hp_X]/1.1mL
  • EQUISETUM HYEMALE 12 [hp_X]/1.1mL
  • FERROUS IODIDE 3 [hp_X]/1.1mL
  • FUMARIA OFFICINALIS FLOWERING TOP 4 [hp_X]/1.1mL
  • GENTIANA LUTEA ROOT 5 [hp_X]/1.1mL
  • GERANIUM ROBERTIANUM 4 [hp_X]/1.1mL
  • MYOSOTIS ARVENSIS 3 [hp_X]/1.1mL
  • NASTURTIUM OFFICINALE 4 [hp_X]/1.1mL
  • PINUS SYLVESTRIS LEAFY TWIG 4 [hp_X]/1.1mL
  • SCROPHULARIA NODOSA 3 [hp_X]/1.1mL
  • SMILAX ORNATA ROOT 6 [hp_X]/1.1mL
  • SODIUM SULFATE 4 [hp_X]/1.1mL
  • TEUCRIUM SCORODONIA FLOWERING TOP 3 [hp_X]/1.1mL
  • THYROID, UNSPECIFIED 12 [hp_X]/1.1mL
  • TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/1.1mL
  • VERONICA OFFICINALIS FLOWERING TOP 3 [hp_X]/1.1mL
    • Pharmacologic Class(es):
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Cations, Divalent - [CS]
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    07-31-2014
    End Marketing Date:
    08-31-2024
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    50114-8200-110 AMPULE in 1 CARTON / 1.1 mL in 1 AMPULE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50114-8200-3?

    The NDC Packaged Code 50114-8200-3 is assigned to a package of 3 ampule in 1 carton / 1.1 ml in 1 ampule of Lymphomyosot X, a human prescription drug labeled by Medinatura. The product's dosage form is injection and is administered via intradermal; intramuscular; intravenous; subcutaneous form.

    Is NDC 50114-8200 included in the NDC Directory?

    Yes, Lymphomyosot X with product code 50114-8200 is active and included in the NDC Directory. The product was first marketed by Medinatura on July 31, 2014.

    What is the 11-digit format for NDC 50114-8200-3?

    The 11-digit format is 50114820003. 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
    5-4-150114-8200-35-4-250114-8200-03