43742-2324 NDC - ADEPS SUILLUS, BRYONIA (ALBA), CALCAREA PHOSPHORICA, CHOLINUM, DESOXYRIBONUCLEIUCUM ACIDUM, DOPAMINE (HYDROCHLORIDE), FERRUM PHOSPHORICUM, FOLIC ACID, INSULINUM, LEPTIN, MAGNESIA MURIATICA, L-METHIONINE, METHYLCOBALAMIN, PROTEUS (VULGARIS), RHUS TOX, RIBOFLAVINUM, RUTA GRAVEOLENS, SACCHARUM OFFICINALE, THIOSINAMINUM, ZINCUM METALLICUM

Drug Information

  • Product NDC: 43742-2324
  • Proprietary Name:
  • Non Proprietary Name: Adeps Suillus, Bryonia (Alba), Calcarea Phosphorica, Cholinum, Desoxyribonucleiucum Acidum, Dopamine (Hydrochloride), Ferrum Phosphoricum, Folic Acid, Insulinum, Leptin, Magnesia Muriatica, L-Methionine, Methylcobalamin, Proteus (Vulgaris), Rhus Tox, Riboflavinum, Ruta Graveolens, Saccharum Officinale, Thiosinaminum, Zincum Metallicum
  • Active Ingredient(s): 300 [hp_X]/mL ALLYLTHIOUREA; 300 [hp_X]/mL BRYONIA ALBA ROOT; 300 [hp_X]/mL CHOLINE HYDROXIDE; 300 [hp_X]/mL DOPAMINE HYDROCHLORIDE; 300 [hp_X]/mL FERROSOFERRIC PHOSPHATE; 300 [hp_X]/mL FOLIC ACID; 300 [hp_X]/mL HERRING SPERM DNA; 300 [hp_X]/mL INSULIN HUMAN; 300 [hp_X]/mL LARD; 300 [hp_X]/mL LEPTIN HUMAN; 300 [hp_X]/mL MAGNESIUM CHLORIDE; 300 [hp_X]/mL METHIONINE; 300 [hp_X]/mL METHYLCOBALAMIN; 300 [hp_X]/mL PROTEUS VULGARIS; 300 [hp_X]/mL RIBOFLAVIN; 300 [hp_X]/mL RUTA GRAVEOLENS FLOWERING TOP; 300 [hp_X]/mL SUCROSE; 300 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF; 300 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE; 300 [hp_X]/mL ZINC
  • Administration Route(s):
  • Dosage Form(s): LIQUID

Labeler Information

Field Name Field Value
Labeler Name: Deseret Biologicals,Inc.
Product Type: DRUG FOR FURTHER PROCESSING
FDA Application Number:
Marketing Category: DRUG FOR FURTHER PROCESSING
Start Marketing Date:4/28/2026

Package Information

No. Package Code Package Description Billing Unit
143742-2324-1960 mL in 1 CONTAINER (43742-2324-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-2324The 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 NAMEDRUG FOR FURTHER PROCESSINGIndicates 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.
NON PROPRIETARY NAMEAdeps Suillus, Bryonia (Alba), Calcarea Phosphorica, Cholinum, Desoxyribonucleiucum Acidum, Dopamine (Hydrochloride), Ferrum Phosphoricum, Folic Acid, Insulinum, Leptin, Magnesia Muriatica, L-Methionine, Methylcobalamin, Proteus (Vulgaris), Rhus Tox, Riboflavinum, Ruta Graveolens, Saccharum Officinale, Thiosinaminum, Zincum MetallicumThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
START MARKETING DATE4/28/2026This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEDRUG FOR FURTHER PROCESSINGProduct 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 NAMEDeseret Biologicals,Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALLYLTHIOUREA; BRYONIA ALBA ROOT; CHOLINE HYDROXIDE; DOPAMINE HYDROCHLORIDE; FERROSOFERRIC PHOSPHATE; FOLIC ACID; HERRING SPERM DNA; INSULIN HUMAN; LARD; LEPTIN HUMAN; MAGNESIUM CHLORIDE; METHIONINE; METHYLCOBALAMIN; PROTEUS VULGARIS; RIBOFLAVIN; RUTA GRAVEOLENS FLOWERING TOP; SUCROSE; TOXICODENDRON PUBESCENS LEAF; TRIBASIC CALCIUM PHOSPHATE; ZINCAn 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 STRENGTH300; 300; 300; 300; 300; 300; 300; 300; 300; 300; 300; 300; 300; 300; 300; 300; 300; 300; 300; 300 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 5/7/2026

Previous Code
Next Code