| Drug NDC: | 64578-0076 |
| The 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. | |
| Proprietary Name: | Thyro-chord |
| Also known as the trade name. It is the name of the product chosen by the labeler. | |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. | |
| Non Proprietary Name: | Homeopathic Liquid |
| Also known as the generic name, this is usually the active ingredient(s) of the product. | |
| Labeler Name: | Energetix Corporation |
| Name of Company corresponding to the labeler code segment of the ProductNDC. | |
| Dosage Form: | Liquid |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. | |
| Substance Name: | .ALPHA.-KETOGLUTARIC ACID - 12 [hp_X]/59.1mL ACETIC ACID - 15 [hp_X]/59.1mL AMMONIUM CHLORIDE - 15 [hp_X]/59.1mL ASPARAGUS - 12 [hp_X]/59.1mL CHELIDONIUM MAJUS - 4 [hp_X]/59.1mL COENZYME A - 12 [hp_X]/59.1mL COPPER - 15 [hp_X]/59.1mL ECHINACEA ANGUSTIFOLIA - 4 [hp_X]/59.1mL FERROUS IODIDE - 12 [hp_X]/59.1mL FUCUS VESICULOSUS - 6 [hp_X]/59.1mL Load more... FUMARIC ACID - 12 [hp_X]/59.1mL GENTIANA LUTEA ROOT - 4 [hp_X]/59.1mL GLYCYRRHIZA GLABRA - 4 [hp_X]/59.1mL GOLD - 15 [hp_X]/59.1mL IODINE - 8 [hp_X]/59.1mL MERCURIUS SOLUBILIS - 15 [hp_X]/59.1mL NADIDE - 12 [hp_X]/59.1mL OYSTER SHELL CALCIUM CARBONATE, CRUDE - 12 [hp_X]/59.1mL PALLADIUM - 15 [hp_X]/59.1mL PERSICARIA PUNCTATA - 12 [hp_X]/59.1mL PHOSPHORIC ACID - 12 [hp_X]/59.1mL POTASSIUM IODIDE - 12 [hp_X]/59.1mL PULSATILLA VULGARIS - 12 [hp_X]/59.1mL RANCID BEEF - 12 [hp_X]/59.1mL SAGE - 8 [hp_X]/59.1mL SILICON DIOXIDE - 12 [hp_X]/59.1mL SILVER - 15 [hp_X]/59.1mL SODIUM DIETHYL OXALACETATE - 12 [hp_X]/59.1mL SODIUM PYRUVATE - 12 [hp_X]/59.1mL SUCCINIC ACID - 12 [hp_X]/59.1mL THYROID, UNSPECIFIED - 9 [hp_X]/59.1mL TIN - 15 [hp_X]/59.1mL VANADIUM - 15 [hp_X]/59.1mL ZINC OXIDE - 15 [hp_X]/59.1mL |
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. | |
| Route Details: | ORAL |
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. | |
| Marketing Start Date: | 08 Sep, 2017 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 25 Dec, 2025 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. | |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. | |
| Manufacturer Name: | Energetix Corporation |
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. | |
| Original Packager: | Yes |
| Whether or not the drug has been repackaged for distribution. | |
| NUI: | N0000185371 N0000175629 N0000184306 M0000728 M0006342 M0022575 M0005152 N0000175831 N0000008595 N0000008924 N0000175830 N0000185375 M0016962 N0000185508 |
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). | |
| UNII: | 8ID597Z82X Q40Q9N063P 01Q9PC255D Z1EJP3037Z 7E889U5RNN SAA04E81UX 789U1901C5 VB06AV5US8 F5452U54PN 535G2ABX9M Load more... 88XHZ13131 S72O3284MS 2788Z9758H 79Y1949PYO 9679TC07X4 324Y4038G2 0U46U6E8UK 2E32821G6I 5TWQ1V240M D32E7AXD4R E4GA8884NN 1C4QK22F9J I76KB35JEV 29SUH5R3HU 065C5D077J ETJ7Z6XBU4 3M4G523W1G 6CA025Y4FG POD38AIF08 AB6MNQ6J6L 0B4FDL9I6P 387GMG9FH5 00J9J9XKDE SOI2LOH54Z |
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. | |
| Pharmacologic Class EPC: | Non-Standardized Food Allergenic Extract [EPC] Copper-containing Intrauterine Device [EPC] Non-Standardized Plant Allergenic Extract [EPC] Standardized Chemical Allergen [EPC] |
| Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`. | |
| Pharmacologic Class PE: | Increased Histamine Release [PE] Cell-mediated Immunity [PE] Decreased Embryonic Implantation [PE] Decreased Sperm Motility [PE] Inhibit Ovum Fertilization [PE] |
| Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`. | |
| Pharmacologic Class CS: | Allergens [CS] Dietary Proteins [CS] Vegetable Proteins [CS] Copper [CS] Plant Proteins [CS] |
| Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient]. | |
| Pharmacologic Class: | Allergens [CS] Cell-mediated Immunity [PE] Copper Absorption Inhibitor [EPC] Copper [CS] Copper-containing Intrauterine Device [EPC] Decreased Copper Ion Absorption [PE] Decreased Embryonic Implantation [PE] Decreased Sperm Motility [PE] Dietary Proteins [CS] Increased Histamine Release [PE] Inhibit Ovum Fertilization [PE] Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] Plant Proteins [CS] Standardized Chemical Allergen [EPC] Vegetable Proteins [CS] |
| These are the reported pharmacological class categories corresponding to the SubstanceNames listed above. | |
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|---|---|---|---|
| 64578-0076-1 | 59.1 mL in 1 BOTTLE, DROPPER (64578-0076-1) | 08 Sep, 2017 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. | ||||
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