NDC codes

FDA NDC Directory
Product NDC (as listed)64578-0101Labeler and product segments. Claims need a package NDC.
Product NDC at billing width64578-0101Add 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 NDC11-digit (billing)PackageCopy
64578-0101-1645780101016457801010159.1 mL in 1 BOTTLE, DROPPER (64578-0101-1)Marketed from Mar 24, 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)
Endocrinpath
Generic name (nonproprietary)
alfalfa, borago officinalis, calcarea carbonica, ceanothus americanus, citricum acidum, fucus vesiculosus, ginkgo biloba, glandula suprarenalis suis, glycyrrhiza glabra, hydrocotyle asiatica, hypothalamus (bovine), kali phosphoricum, pancreas suis, phytolacca decandra, pituitarum posterium (bovine), sarsaparilla (smilax regelii), silicea, syzygium jambolanum, taraxacum officinale, thyroidinum (bovine)
Active ingredients
Alfalfa — 15 [hp_X]/mLBorage — 15 [hp_X]/mLOyster shell calcium carbonate, Crude — 15 [hp_X]/mLCeanothus americanus leaf — 4 [hp_X]/mLAnhydrous citric acid — 15 [hp_X]/mLFucus vesiculosus — 15 [hp_X]/mLGinkgo — 15 [hp_X]/mLSus scrofa adrenal gland — 9 [hp_X]/mLGlycyrrhiza glabra — 15 [hp_X]/mLCentella asiatica — 15 [hp_X]/mLBos taurus hypothalamus — 12 [hp_X]/mLPotassium phosphate, Dibasic — 15 [hp_X]/mLSus scrofa pancreas — 9 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLBos taurus pituitary gland — 12 [hp_X]/mLSmilax ornata root — 15 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLSyzygium cumini seed — 4 [hp_X]/mLTaraxacum officinale — 15 [hp_X]/mLThyroid, Bovine — 9 [hp_X]/mL
Dosage form
Liquid
Route
Oral
Labeler
Energetix CorporationNDC labeler code 64578
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Acidifying Activity (Mechanism)Allergens (Chemical structure)Calcium Chelating Activity (Mechanism)Cell-mediated Immunity (Physiologic effect)Decreased Coagulation Factor Activity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers
Product ID 64578-0101_2903c974-3b8f-7e01-e063-6294a90adc0bSPL ID 2903c974-3b8f-7e01-e063-6294a90adc0bSPL set ID 70f84941-b8a1-48f4-9c05-554e554f0049UNII DJO934BRBD, PB618V0K2W, 2E32821G6I, 25B1Y14T8N, XF417D3PSL, 535G2ABX9M, 19FUJ2C58T, 398IYQ16YV, 2788Z9758H, 7M867G6T1U, S6G2NLH4Y7, CI71S98N1Z, 9Y3J3362RY, 11E6VI8VEG, 7JM57I419K, 2H1576D5WG, ETJ7Z6XBU4, 820LSF646I, 39981FM375, MN18OTN73W
Pharmacologic class
Anti-coagulant; Calculi Dissolution Agent; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N464578010101 followed by a unit qualifier and the quantity

Package 64578-0101-01. 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 .

Indications (excerpt from the label)

Uses Temporary relief of weakness, craving for sweets, irritability.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 64578-0101

What is NDC 64578-0101?
64578-0101 is the product NDC for Endocrinpath, Alfalfa 15 [hp_X]/mL + 19 more ingredients liquid, listed with the FDA by Energetix Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Endocrinpath (Alfalfa, Borago Officinalis, Calcarea Carbonica, Ceanothus Americanus, Citricum Acidum, Fucus Vesiculosus, Ginkgo Biloba, Glandula Suprarenalis Suis, Glycyrrhiza Glabra, Hydrocotyle Asiatica, Hypothalamus (Bovine), Kali Phosphoricum, Pancreas Suis, Phytolacca Decandra, Pituitarum Posterium (Bovine), Sarsaparilla (Smilax Regelii), Silicea, Syzygium Jambolanum, Taraxacum Officinale, Thyroidinum (Bovine)).
What is the active ingredient?
Alfalfa, Borage, Oyster shell calcium carbonate, Crude, Ceanothus americanus leaf, Anhydrous citric acid, Fucus vesiculosus, Ginkgo, Sus scrofa adrenal gland, Glycyrrhiza glabra, Centella asiatica, Bos taurus hypothalamus, Potassium phosphate, Dibasic, Sus scrofa pancreas, Phytolacca americana root, Bos taurus pituitary gland, Smilax ornata root, Silicon dioxide, Syzygium cumini seed, Taraxacum officinale, Thyroid, Bovine.
Who is the labeler?
Energetix Corporation, NDC labeler code 64578. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Endocrinpath?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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