Adaptopath NDC 64578-0095

NDC codes

FDA NDC Directory

Product NDC (as listed)64578-0095Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64578-0095Add 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
64578-0095-1	64578009501	59.1 mL in 1 BOTTLE, DROPPER (64578-0095-1)Marketed from May 23, 2016

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): Adaptopath
Generic name (nonproprietary): adenosinum cyclophosphoricum, alpha-lipoicum acidum, argentum metallicum, avena sativa, capsicum annuum, citricum acidum, coenzyme a, cuprum metallicum, ginkgo biloba, glandula suprarenalis suis, glycyrrhiza glabra, hypothalamus (bovine), iodium, ledum palustre, manganum aceticum, nadidum, natrum carbonicum, oleum morrhuae, phosphoricum acidum, picricum acidum, riboflavinum, selenium metallicum sepia, silicea, thiaminum hydrochloricum, thyroidinum (bovine), vanadium metallicum
Active ingredients: Adenosine cyclic phosphate — 8 [hp_X]/mL.alpha.-lipoic acid — 12 [hp_X]/mLSilver — 12 [hp_X]/mLAvena sativa flowering top — 4 [hp_X]/mLCapsicum — 4 [hp_X]/mLAnhydrous citric acid — 4 [hp_X]/mLCoenzyme a — 8 [hp_X]/mLCopper — 12 [hp_X]/mLGinkgo — 4 [hp_X]/mLSus scrofa adrenal gland — 9 [hp_X]/mLGlycyrrhiza glabra — 4 [hp_X]/mLBos taurus hypothalamus — 12 [hp_X]/mLIodine — 12 [hp_X]/mLLedum palustre twig — 6 [hp_X]/mLManganese acetate tetrahydrate — 12 [hp_X]/mLNadide — 12 [hp_X]/mLSodium carbonate — 12 [hp_X]/mLCod liver oil — 6 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLPicric acid — 12 [hp_X]/mLRiboflavin — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLThiamine hydrochloride — 8 [hp_X]/mLThyroid, Bovine — 9 [hp_X]/mLVanadium — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energetix Corporation
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 22, 2014
Listing expires: Dec 31, 2027
Other FDA classes: Acidifying Activity (Mechanism)Allergens (Chemical structure)Allergens (Chemical structure)Calcium Chelating Activity (Mechanism)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Copper (Chemical structure)Decreased Coagulation Factor Activity (Physiologic effect)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)Magnetic Resonance Contrast Activity (Mechanism)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 64578-0095_58c7f5f1-7361-86e8-e063-6394a90a2a1fSPL ID 58c7f5f1-7361-86e8-e063-6394a90a2a1fSPL set ID 41234598-0cb5-41c2-bfbe-1c15ee9bf502UNII E0399OZS9N, 73Y7P0K73Y, 3M4G523W1G, MA9CQJ3F7F, 00UK7646FG, XF417D3PSL, SAA04E81UX, 789U1901C5, 19FUJ2C58T, 398IYQ16YV, 2788Z9758H, S6G2NLH4Y7, 9679TC07X4, 877L01IZ0P, 9TO51D176N, 0U46U6E8UK, 45P3261C7T, BBL281NWFG, E4GA8884NN, A49OS0F91S, TLM2976OFR, H6241UJ22B, QDL83WN8C2, ETJ7Z6XBU4, M572600E5P, MN18OTN73W, 00J9J9XKDE
Pharmacologic class: Anti-coagulant; Calculi Dissolution Agent; Copper-containing Intrauterine Device; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Paramagnetic Contrast Agent

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

N464578009501 followed by a unit qualifier and the quantity

Package 64578-0095-01. 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 low energy, sluggish digestion, muscle weakness.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)