Aacg-a, Aacg-b, Adenosinum Cyclophosphoricum, Berberinum, Calcarea Carbonica, Cinchona Officinalis, Cholinum, Colibacillinum Cum Natrum Muriaticum, Curcuma Longa, Methylcobalamin, Dna, Ferrum Metallicum, Panax Ginseng, L-glutamic Acid, Hepar Suis, Hypothalamus Suis, Indolum, Insulinum, Iodium, Lycopodium Clavatum, Magnesia Carbonica, L-methionine, Pancreas Suis, Stomach (suis), Zincum Metallicum, 7-oxo-dehydroepiandrosterone-3b-acetate Liquid
NDC 43742-2311
View dosage, usage, ingredients, routes, and UNII mappings.
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.
Aacg-a, Aacg-b, Adenosinum Cyclophosphoricum, Berberinum, Calcarea Carbonica, Cinchona Officinalis, Cholinum, Colibacillinum Cum Natrum Muriaticum, Curcuma Longa, Methylcobalamin, Dna, Ferrum Metallicum, Panax Ginseng, L-glutamic Acid, Hepar Suis, Hypothalamus Suis, Indolum, Insulinum, Iodium, Lycopodium Clavatum, Magnesia Carbonica, L-methionine, Pancreas Suis, Stomach (suis), Zincum Metallicum, 7-oxo-dehydroepiandrosterone-3b-acetate is a DRUG FOR FURTHER PROCESSING-approved product labeled by Deseret Biologicals,inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a liquid. This product entry covers the primary NDC 43742-2311 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
43742-2311
Proprietary Name:
Aacg-a, Aacg-b, Adenosinum Cyclophosphoricum, Berberinum, Calcarea Carbonica, Cinchona Officinalis, Cholinum, Colibacillinum Cum Natrum Muriaticum, Curcuma Longa, Methylcobalamin, Dna, Ferrum Metallicum, Panax Ginseng, L-glutamic Acid, Hepar Suis, Hypothalamus Suis, Indolum, Insulinum, Iodium, Lycopodium Clavatum, Magnesia Carbonica, L-methionine, Pancreas Suis, Stomach (suis), Zincum Metallicum, 7-oxo-dehydroepiandrosterone-3b-acetate
Non-Proprietary Name: [1]
Aacg-a, Aacg-b, Adenosinum Cyclophosphoricum, Berberinum, Calcarea Carbonica, Cinchona Officinalis, Cholinum, Colibacillinum Cum Natrum Muriaticum, Curcuma Longa, Methylcobalamin, Dna, Ferrum Metallicum, Panax Ginseng, L-glutamic Acid, Hepar Suis, Hypothalamus Suis, Indolum, Insulinum, Iodium, Lycopodium Clavatum, Magnesia Carbonica, L-methionine, Pancreas Suis, Stomach (suis), Zincum Metallicum, 7-oxo-dehydroepiandrosterone-3b-acetate
Substance Name: [2]
7-keto-dehydroepiandrosterone; Adenosine Cyclic Phosphate; Apc-356433; Apc-356434; Asian Ginseng; Berberine Chloride; Choline Hydroxide; Cinchona Officinalis Bark; Escherichia Coli; Glutamic Acid; Herring Sperm Dna; Indole; Insulin Human; Iodine; Iron; Lycopodium Clavatum Spore; Magnesium Carbonate; Methionine; Methylcobalamin; Oyster Shell Calcium Carbonate, Crude; Pork Liver; Sus Scrofa Hypothalamus; Sus Scrofa Pancreas; Sus Scrofa Stomach; Turmeric; Zinc
NDC Directory Status:
Drug For Further Processing
Product Type: [3]
UNFINISHED PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
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 & Regulatory Data
Labeler Name: [5]
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.
Marketing Timeline
Start Marketing Date: [9]
04-06-2026
Listing Expiration Date: [11]
12-31-2027
Exclude Flag: [12]
N
Unfinished Product: [13]
Yes
Code Structure Chart
Product Details
What is NDC 43742-2311?
The NDC code 43742-2311 is assigned by the FDA to the product Aacg-a, Aacg-b, Adenosinum Cyclophosphoricum, Berberinum, Calcarea Carbonica, Cinchona Officinalis, Cholinum, Colibacillinum Cum Natrum Muriaticum, Curcuma Longa, Methylcobalamin, Dna, Ferrum Metallicum, Panax Ginseng, L-glutamic Acid, Hepar Suis, Hypothalamus Suis, Indolum, Insulinum, Iodium, Lycopodium Clavatum, Magnesia Carbonica, L-methionine, Pancreas Suis, Stomach (suis), Zincum Metallicum, 7-oxo-dehydroepiandrosterone-3b-acetate. It is commonly known by its generic name, aacg-a, aacg-b, adenosinum cyclophosphoricum, berberinum, calcarea carbonica, cinchona officinalis, cholinum, colibacillinum cum natrum muriaticum, curcuma longa, methylcobalamin, dna, ferrum metallicum, panax ginseng, l-glutamic acid, hepar suis, hypothalamus suis, indolum, insulinum, iodium, lycopodium clavatum, magnesia carbonica, l-methionine, pancreas suis, stomach (suis), zincum metallicum, 7-oxo-dehydroepiandrosterone-3b-acetate. This pharmaceutical product is labeled by Deseret Biologicals,inc. and is currently categorized as listed product. The medication is a liquid. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 43742-2311-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are Active Ingredients of this product?
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.
- 7-KETO-DEHYDROEPIANDROSTERONE 35 [hp_X]/mL
- ADENOSINE CYCLIC PHOSPHATE 35 [hp_X]/mL
- APC-356433 35 [hp_X]/mL
- APC-356434 35 [hp_X]/mL
- ASIAN GINSENG 35 [hp_X]/mL
- BERBERINE CHLORIDE 35 [hp_X]/mL
- CHOLINE HYDROXIDE 35 [hp_X]/mL - A basic constituent of lecithin that is found in many plants and animal organs. It is important as a precursor of acetylcholine, as a methyl donor in various metabolic processes, and in lipid metabolism.
- CINCHONA OFFICINALIS BARK 35 [hp_X]/mL
- ESCHERICHIA COLI 35 [hp_X]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc.
- GLUTAMIC ACID 35 [hp_X]/mL - A non-essential amino acid naturally occurring in the L-form. Glutamic acid is the most common excitatory neurotransmitter in the CENTRAL NERVOUS SYSTEM.
- HERRING SPERM DNA 35 [hp_X]/mL
- INDOLE 35 [hp_X]/mL - Benzopyrroles with the nitrogen at the number one carbon adjacent to the benzyl portion, in contrast to ISOINDOLES which have the nitrogen away from the six-membered ring.
- INSULIN HUMAN 35 [hp_X]/mL
- IODINE 35 [hp_X]/mL - A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
- IRON 35 [hp_X]/mL - A metallic element with atomic symbol Fe, atomic number 26, and atomic weight 55.85. It is an essential constituent of HEMOGLOBINS; CYTOCHROMES; and IRON-BINDING PROTEINS. It plays a role in cellular redox reactions and in the transport of OXYGEN.
- LYCOPODIUM CLAVATUM SPORE 35 [hp_X]/mL
- MAGNESIUM CARBONATE 35 [hp_X]/mL - RN given refers to parent cpd (1:1)
- METHIONINE 35 [hp_X]/mL - A sulfur-containing essential L-amino acid that is important in many body functions.
- METHYLCOBALAMIN 35 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 35 [hp_X]/mL
- PORK LIVER 35 [hp_X]/mL
- SUS SCROFA HYPOTHALAMUS 35 [hp_X]/mL
- SUS SCROFA PANCREAS 35 [hp_X]/mL
- SUS SCROFA STOMACH 35 [hp_X]/mL
- TURMERIC 35 [hp_X]/mL
- ZINC 35 [hp_X]/mL - A metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.
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Product & Regulatory Definitions
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.
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.
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.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
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.
