Terrestristat NDC 44911-0677

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0677Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0677Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
44911-0677-1	44911067701	30 mL in 1 BOTTLE, DROPPER (44911-0677-1)Marketed from Nov 17, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Terrestristat
Generic name (nonproprietary): alfalfa, avena sativa, fucus vesiculosus, aralia quinquefolia, natrum carbonicum, thyroidinum (suis), cerebrum suis, pineal gland (suis), rhododendron chrysanthum, agate, argentum nitricum, cadmium iodatum, calcarea phosphorica, coffea cruda, cuprum metallicum, mercurius corrosivus, phosphoricum acidum, phosphorus, quartz, silicea, strontium carbonicum, radium bromatum, carcinosin, tarentula cubensis, x-ray, holmium metallicum, uranium nitricum.
Active ingredients: Medicago sativa whole — 3 [hp_X]/mLAvena sativa flowering top — 3 [hp_X]/mLFucus vesiculosus — 3 [hp_X]/mLAmerican ginseng — 6 [hp_X]/mLSodium carbonate — 6 [hp_X]/mLThyroid — 6 [hp_X]/mLSus scrofa cerebrum — 8 [hp_X]/mLSus scrofa pineal gland — 8 [hp_X]/mLRhododendron aureum leaf — 10 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLSilver nitrate — 12 [hp_X]/mLCadmium iodide — 12 [hp_X]/mLTribasic calcium phosphate — 12 [hp_X]/mLArabica coffee bean — 12 [hp_X]/mLCopper — 12 [hp_X]/mLMercuric chloride — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLStrontium carbonate — 12 [hp_X]/mLRadium bromide — 16 [hp_X]/mLHuman breast tumor cell — 30 [hp_X]/mLCitharacanthus spinicrus — 30 [hp_X]/mLAlcohol, X-ray exposed (1000 rad) — 30 [hp_X]/mLHolmium — 12 [hp_C]/mLUranyl nitrate hexahydrate — 15 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 17, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Dietary Proteins (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Phosphate Chelating Activity (Mechanism)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 44911-0677_a7ece306-3ce3-4bae-b410-4ae48239524dSPL ID a7ece306-3ce3-4bae-b410-4ae48239524dSPL set ID 9bd83312-6872-4e39-b7ff-bbeb69015d80UNII DJO934BRBD, MA9CQJ3F7F, 535G2ABX9M, 8W75VCV53Q, 45P3261C7T, 6RV024OAUQ, 4GB5DQR532, 050QZ2EDK7, IV92NQJ73U, ETJ7Z6XBU4, 95IT3W8JZE, 2F2UPU4KCW, 91D9GV0Z28, 3SW678MX72, 789U1901C5, 53GH7MZT1R, E4GA8884NN, 27YLU75U4W, 41YPU4MMCA, R74O7T8569, C62OO7VD9K, 3Y5X6RT823, 6PRJ93602P, W1XX32SQN1, 3V057702FYUPC 0363113700190
Pharmacologic class: Blood Coagulation Factor; Copper-containing Intrauterine Device; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Phosphate Binder

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N444911067701 followed by a unit qualifier and the quantity

Package 44911-0677-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Nov 17, 2023.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve nervousness, anxiety, restlessness, weakness, trembling, numbness, and skin eruptions and cracking.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)