Lipo-Chord NDC 64578-0145

NDC codes

FDA NDC Directory

Product NDC (as listed)64578-0145Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64578-0145Add 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
64578-0145-1	64578014501	59.1 mL in 1 BOTTLE, DROPPER (64578-0145-1)Marketed from Aug 18, 2017

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): Lipo-Chord
Generic name (nonproprietary): aceticum ac, acetylsal ac, adrenocorticotrophin, alumina, arsenicum alb, borago, ceanothus, chelidonium maj, chionanthus, chloramphenicolum, chlorpromazinum, cholesterinum, cortisone aceticum, damiana, folliculinum, fumaricum ac, kali iod, lycopodium, nat sulphuricum, nux vom, oleum morrhuae, petroleum, phenacetinum, phosphoricum ac, phosphorus, plumb met, saccharum off, silicea, taraxacum, thyroidinum.
Active ingredients: Acetic acid — 18 [hp_X]/59.1mLAspirin — 18 [hp_X]/59.1mLCorticotropin human — 18 [hp_X]/59.1mLAluminum oxide — 18 [hp_X]/59.1mLArsenic trioxide — 30 [hp_X]/59.1mLBorage — 6 [hp_X]/59.1mLCeanothus americanus leaf — 6 [hp_X]/59.1mLChelidonium majus — 12 [hp_X]/59.1mLChionanthus virginicus bark — 6 [hp_X]/59.1mLChloramphenicol — 18 [hp_X]/59.1mLChlorpromazine — 18 [hp_X]/59.1mLCholesterol — 12 [hp_X]/59.1mLCortisone acetate — 18 [hp_X]/59.1mLTurnera diffusa leafy twig — 12 [hp_X]/59.1mLEstrone — 18 [hp_X]/59.1mLFumaric acid — 30 [hp_X]/59.1mLPotassium iodide — 30 [hp_X]/59.1mLLycopodium clavatum spore — 30 [hp_X]/59.1mLSodium sulfate — 30 [hp_X]/59.1mLStrychnos nux-vomica seed — 30 [hp_X]/59.1mLCod liver oil — 12 [hp_X]/59.1mLKerosene — 18 [hp_X]/59.1mLPhenacetin — 18 [hp_X]/59.1mLPhosphoric acid — 30 [hp_X]/59.1mLPhosphorus — 30 [hp_X]/59.1mLLead — 30 [hp_X]/59.1mLSucrose — 30 [hp_X]/59.1mLSilicon dioxide — 30 [hp_X]/59.1mLTaraxacum officinale — 4 [hp_X]/59.1mLThyroid, Unspecified — 9 [hp_X]/59.1mL
Dosage form: Liquid
Route: Oral
Labeler: Energetix Corporation
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 18, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Amphenicols (EXT)Non-Steroidal (Chemical structure)Cell-mediated Immunity (Physiologic effect)Corticosteroid Hormone Receptor Agonists (Mechanism)Cyclooxygenase Inhibitors (Mechanism)Decreased Platelet Aggregation (Physiologic effect)Decreased Prostaglandin Production (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Phenothiazines (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 64578-0145_58c983c5-dadb-bab7-e063-6394a90a232dSPL ID 58c983c5-dadb-bab7-e063-6394a90a232dSPL set ID 5c83cbd5-46fb-48a0-a739-ff9c81e7129cUNII Q40Q9N063P, R16CO5Y76E, 63KF469V7T, LMI26O6933, S7V92P67HO, PB618V0K2W, 25B1Y14T8N, 7E889U5RNN, 66974FR9Q1, U42B7VYA4P, 97C5T2UQ7J, 883WKN7W8X, RQ2CFA7WWJ, 2DI9HA706A, 88XHZ13131, 1C4QK22F9J, C88X29Y479, 0YPR65R21J, 269XH13919, BBL281NWFG, 1C89KKC04E, ER0CTH01H9, E4GA8884NN, 27YLU75U4W, 2P299V784P, C151H8M554, ETJ7Z6XBU4, 39981FM375, 0B4FDL9I6P
Pharmacologic class: Amphenicol-class Antibacterial; Corticosteroid; Non-Standardized Plant Allergenic Extract; Nonsteroidal Anti-inflammatory Drug; Phenothiazine; Platelet Aggregation Inhibitor

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

N464578014501 followed by a unit qualifier and the quantity

Package 64578-0145-01. 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 Aug 11, 2026.

Indications (excerpt from the label)

Uses Temporary relief of weakness, abdominal bloating, fatigue.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)