0220-7309 NDC - MEDORRHINUM (GONORRHEAL URETHRAL SECRETION HUMAN)

Drug Information

Product NDC: 0220-7309

Proprietary Name: Medorrhinum

Non Proprietary Name: GONORRHEAL URETHRAL SECRETION HUMAN

Active Ingredient(s):
  • 12 [hp_X]/1 GONORRHEAL URETHRAL SECRETION HUMAN


Administration Route(s): ORAL

Dosage Form(s): PELLET

Labeler Information

Labeler Name: Laboratoires Boiron
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/3/1983

Package Information

No. Package Code Package Description Billing Unit
10220-7309-4180 PELLET in 1 TUBE (0220-7309-41)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0220-7309The 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 NAMEMedorrhinumThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEGONORRHEAL URETHRAL SECRETION HUMANThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPELLETThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE3/3/1983This 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 NAMELaboratoires BoironName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEGONORRHEAL URETHRAL SECRETION HUMANAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH12 
ACTIVE INGRED UNIT[hp_X]/1 

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This page was last updated on: 2/1/2023