0360-0150 NDC - CUPRUM METALLICUM (CUPRUM MET.)

Drug Information

Product NDC: 0360-0150

Proprietary Name: CUPRUM METALLICUM

Non Proprietary Name: CUPRUM MET.

Active Ingredient(s):
  • 30 [hp_X]/g COPPER


Administration Route(s): SUBLINGUAL

Dosage Form(s): TABLET

Pharmacy Class(es):
  • Copper [CS];
  • Copper-containing Intrauterine Device [EPC];
  • Decreased Embryonic Implantation [PE];
  • Decreased Sperm Motility [PE];
  • Inhibit Ovum Fertilization [PE]

Labeler Information

Labeler Name: STANDARD HOMEOPATHIC COMPANY
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:2/17/1997

Package Information

No. Package Code Package Description Billing Unit
10360-0150-011 g in 1 BOTTLE, PLASTIC (0360-0150-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0360-0150The 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 OTC 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 NAMECUPRUM METALLICUMThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECUPRUM MET.The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLETThe translation of the dosage form Code submitted by the firm.
ROUTE NAMESUBLINGUALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE2/17/1997This 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 NAMESTANDARD HOMEOPATHIC COMPANYName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECOPPERAn 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 STRENGTH30 
ACTIVE INGRED UNIT[hp_X]/g 
PHARM CLASSESCopper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [PE] 

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