52919-123 NDC - LYMPHOMYOSOT (GERANIUM ROBERTIANUM AND RORIPPA NASTURTIUM-AQUATICUM AND TRIBASIC CALCIUM PHOSPHATE AND LEVOTHYROXINE AND)

Drug Information

Product NDC: 52919-123

Proprietary Name: Lymphomyosot

Non Proprietary Name: GERANIUM ROBERTIANUM and RORIPPA NASTURTIUM-AQUATICUM and TRIBASIC CALCIUM PHOSPHATE and LEVOTHYROXINE and

Active Ingredient(s):
  • 4 [hp_X]/1.1mL GERANIUM ROBERTIANUM;
  • 4 [hp_X]/1.1mL RORIPPA NASTURTIUM-AQUATICUM;
  • 12 [hp_X]/1.1mL FERROUS IODIDE;
  • 3 [hp_X]/1.1mL JUGLANS REGIA FLOWERING TOP;
  • 3 [hp_X]/1.1mL MYOSOTIS ARVENSIS;
  • 3 [hp_X]/1.1mL SCROPHULARIA NODOSA;
  • 3 [hp_X]/1.1mL TEUCRIUM SCORODONIA FLOWERING TOP;
  • 3 [hp_X]/1.1mL VERONICA OFFICINALIS FLOWERING TOP;
  • 4 [hp_X]/1.1mL EQUISETUM HYEMALE;
  • 4 [hp_X]/1.1mL FUMARIA OFFICINALIS FLOWERING TOP;
  • 4 [hp_X]/1.1mL SODIUM SULFATE;
  • 4 [hp_X]/1.1mL PINUS SYLVESTRIS TOP;
  • 5 [hp_X]/1.1mL GENTIANA LUTEA ROOT;
  • 6 [hp_X]/1.1mL ARANEUS DIADEMATUS;
  • 6 [hp_X]/1.1mL SARSAPARILLA;
  • 12 [hp_X]/1.1mL TRIBASIC CALCIUM PHOSPHATE;
  • 12 [hp_X]/1.1mL LEVOTHYROXINE


Administration Route(s): INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS

Dosage Form(s): INJECTION

Pharmacy Class(es):
  • Osmotic Laxative [EPC];
  • Increased Large Intestinal Motility [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Osmotic Activity [MoA];
  • Blood Coagulation Factor [EPC];
  • Increased Coagulation Factor Activity [PE];
  • Calcium [CS];
  • Cations;
  • Divalent [CS];
  • l-Thyroxine [EPC];
  • Thyroxine [CS]

Labeler Information

Labeler Name: Hameln Pharma GmbH
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:4/1/2010

Package Information

No. Package Code Package Description Billing Unit
152919-123-101.1 mL in 1 AMPULE (52919-123-10)

NDC Record

Field Name Field Value Definition
PRODUCT NDC52919-123The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMELymphomyosotThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEGERANIUM ROBERTIANUM and RORIPPA NASTURTIUM-AQUATICUM and TRIBASIC CALCIUM PHOSPHATE and LEVOTHYROXINE andThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEINJECTIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEINTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUSThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE4/1/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEHameln Pharma GmbHName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEGERANIUM ROBERTIANUM; RORIPPA NASTURTIUM-AQUATICUM; FERROUS IODIDE; JUGLANS REGIA FLOWERING TOP; MYOSOTIS ARVENSIS; SCROPHULARIA NODOSA; TEUCRIUM SCORODONIA FLOWERING TOP; VERONICA OFFICINALIS FLOWERING TOP; EQUISETUM HYEMALE; FUMARIA OFFICINALIS FLOWERING TOP; SODIUM SULFATE; PINUS SYLVESTRIS TOP; GENTIANA LUTEA ROOT; ARANEUS DIADEMATUS; SARSAPARILLA; TRIBASIC CALCIUM PHOSPHATE; LEVOTHYROXINEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH4; 4; 12; 3; 3; 3; 3; 3; 4; 4; 4; 4; 5; 6; 6; 12; 12 
ACTIVE INGRED UNIT[hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL 
PHARM CLASSESOsmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS],l-Thyroxine [EPC],Thyroxine [CS] 

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This page was last updated on: 9/13/2019