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  4. NDC Product Code: 43742-1515 Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Folliculinum, Hydrocortisone (cortisol), Petroselinum Sativum, Progesterone, Thyroidinum (suis), Estradiol, Human Growth Hormone, Androsterone, Aldosterone

NDC 43742-1515 Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Folliculinum, Hydrocortisone (cortisol), Petroselinum Sativum, Progesterone, Thyroidinum (suis), Estradiol, Human Growth Hormone, Androsterone, Aldosterone

Liquid - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1515?
  4. Active Ingredients

Product Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.
NDC Product Code:
43742-1515
Proprietary Name:
Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Folliculinum, Hydrocortisone (cortisol), Petroselinum Sativum, Progesterone, Thyroidinum (suis), Estradiol, Human Growth Hormone, Androsterone, Aldosterone
Non-Proprietary Name: [1]
Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Folliculinum, Hydrocortisone (cortisol), Petroselinum Sativum, Progesterone, Thyroidinum (suis), Estradiol, Human Growth Hormone, Androsterone, Aldosterone
Substance Name: [2]
Acetaldehyde; Aldosterone; Androsterone; Cholesterol; Dopamine Hydrochloride; Estradiol; Estrone; Hydrocortisone; Petroselinum Crispum; Progesterone; Somatropin; Sus Scrofa Thyroid
NDC Directory Status:
Drug For Further Processing
Product Type: [3]
UNFINISHED PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Labeler Name: [5]
Deseret Biologicals, Inc.
Labeler Code:
43742
Marketing Category: [8]
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date: [9]
09-11-2019
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Unfinished Product: [13]
Yes
Code Navigator:

Code Structure Chart

Product Details

What is NDC 43742-1515?

The NDC code 43742-1515 is assigned by the FDA to the UNFINISHED product Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Folliculinum, Hydrocortisone (cortisol), Petroselinum Sativum, Progesterone, Thyroidinum (suis), Estradiol, Human Growth Hormone, Androsterone, Aldosterone which is drug for further processing product labeled by Deseret Biologicals, Inc.. The generic name of Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Folliculinum, Hydrocortisone (cortisol), Petroselinum Sativum, Progesterone, Thyroidinum (suis), Estradiol, Human Growth Hormone, Androsterone, Aldosterone is acetaldehyde, cholesterinum, dopamine hydrochloride, folliculinum, hydrocortisone (cortisol), petroselinum sativum, progesterone, thyroidinum (suis), estradiol, human growth hormone, androsterone, aldosterone. The product's dosage form is liquid. The product is distributed in a single package with assigned NDC code 43742-1515-1 960 ml in 1 bottle, plastic . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Folliculinum, Hydrocortisone (cortisol), Petroselinum Sativum, Progesterone, Thyroidinum (suis), Estradiol, Human Growth Hormone, Androsterone, Aldosterone Active Ingredients?

An 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.
  • ACETALDEHYDE 8 [hp_X]/mL - A colorless, flammable liquid used in the manufacture of acetic acid, perfumes, and flavors. It is also an intermediate in the metabolism of alcohol. It has a general narcotic action and also causes irritation of mucous membranes. Large doses may cause death from respiratory paralysis.
  • ALDOSTERONE 34 [hp_C]/mL - A hormone secreted by the ADRENAL CORTEX that regulates electrolyte and water balance by increasing the renal retention of sodium and the excretion of potassium.
  • ANDROSTERONE 15 [hp_C]/mL - A metabolite of TESTOSTERONE or ANDROSTENEDIONE with a 3-alpha-hydroxyl group and without the double bond. The 3-beta hydroxyl isomer is epiandrosterone.
  • CHOLESTEROL 8 [hp_X]/mL - The principal sterol of all higher animals, distributed in body tissues, especially the brain and spinal cord, and in animal fats and oils.
  • DOPAMINE HYDROCHLORIDE 8 [hp_X]/mL - One of the catecholamine NEUROTRANSMITTERS in the brain. It is derived from TYROSINE and is the precursor to NOREPINEPHRINE and EPINEPHRINE. Dopamine is a major transmitter in the extrapyramidal system of the brain, and important in regulating movement. A family of receptors (RECEPTORS, DOPAMINE) mediate its action.
  • ESTRADIOL 12 [hp_X]/mL - The 17-beta-isomer of estradiol, an aromatized C18 steroid with hydroxyl group at 3-beta- and 17-beta-position. Estradiol-17-beta is the most potent form of mammalian estrogenic steroids.
  • ESTRONE 8 [hp_X]/mL - An aromatized C18 steroid with a 3-hydroxyl group and a 17-ketone, a major mammalian estrogen. It is converted from ANDROSTENEDIONE directly, or from TESTOSTERONE via ESTRADIOL. In humans, it is produced primarily by the cyclic ovaries, PLACENTA, and the ADIPOSE TISSUE of men and postmenopausal women.
  • HYDROCORTISONE 8 [hp_X]/mL - The main glucocorticoid secreted by the ADRENAL CORTEX. Its synthetic counterpart is used, either as an injection or topically, in the treatment of inflammation, allergy, collagen diseases, asthma, adrenocortical deficiency, shock, and some neoplastic conditions.
  • PETROSELINUM CRISPUM 8 [hp_X]/mL - A plant genus of the family APIACEAE used for flavoring food.
  • PROGESTERONE 8 [hp_X]/mL - The major progestational steroid that is secreted primarily by the CORPUS LUTEUM and the PLACENTA. Progesterone acts on the UTERUS, the MAMMARY GLANDS and the BRAIN. It is required in EMBRYO IMPLANTATION; PREGNANCY maintenance, and the development of mammary tissue for MILK production. Progesterone, converted from PREGNENOLONE, also serves as an intermediate in the biosynthesis of GONADAL STEROID HORMONES and adrenal CORTICOSTEROIDS.
  • SOMATROPIN 12 [hp_X]/mL - A 191-amino acid polypeptide hormone secreted by the human adenohypophysis (PITUITARY GLAND, ANTERIOR), also known as GH or somatotropin. Synthetic growth hormone, termed somatropin, has replaced the natural form in therapeutic usage such as treatment of dwarfism in children with growth hormone deficiency.
  • SUS SCROFA THYROID 8 [hp_X]/mL

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Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[2] What is the Substance Name? - An 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.

[3] What kind of product is this? - Indicates 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.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] What is the Marketing Category? - Product 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

[13] What is an Unfinished Product? - This field indicates if the product is an unfinished drug. An unfinished drug is an active pharmaceutical ingredient either alone or with other ingredients that is not a finished drug product. Unfinished drugs are used to process other drugs or for drug compounding.