Endopath-F NDC 64578-0170

NDC codes

FDA NDC Directory

Product NDC (as listed)64578-0170Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64578-0170Add 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
64578-0170-1	64578017001	59.1 mL in 1 BOTTLE (64578-0170-1)Marketed from Sep 10, 2015

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): Endopath-F
Generic name (nonproprietary): agnus, angelica sin, cimicifuga, fucus, glandula suprarenalis suis, glycyrrhiza, hypothalamus, oophorinum, pituitarum posterium, pulsatilla, sepia, thyroidinum, xanthoxylum
Active ingredients: Chaste tree fruit — 4 [hp_X]/59.1mLAngelica sinensis root — 8 [hp_X]/59.1mLBlack cohosh — 4 [hp_X]/59.1mLFucus vesiculosus — 4 [hp_X]/59.1mLSus scrofa adrenal gland — 9 [hp_X]/59.1mLLicorice — 4 [hp_X]/59.1mLBos taurus hypothalamus — 12 [hp_X]/59.1mLSus scrofa ovary — 9 [hp_X]/59.1mLSus scrofa pituitary gland, Posterior — 12 [hp_X]/59.1mLPulsatilla vulgaris — 12 [hp_X]/59.1mLSepia officinalis juice — 12 [hp_X]/59.1mLThyroid, Unspecified — 9 [hp_X]/59.1mLZanthoxylum americanum bark — 4 [hp_X]/59.1mL
Dosage form: Liquid
Route: Oral
Labeler: Energetix Corporation
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 10, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 64578-0170_2903c621-c6e2-9048-e063-6394a90a7fa6SPL ID 2903c621-c6e2-9048-e063-6394a90a7fa6SPL set ID d0880c30-54f5-4af4-ad5d-85ecae3bb9e5UNII 433OSF3U8A, B66F4574UG, K73E24S6X9, 535G2ABX9M, 398IYQ16YV, 61ZBX54883, S6G2NLH4Y7, S7YTV04R8O, E8S87O660T, I76KB35JEV, QDL83WN8C2, 0B4FDL9I6P, A4KL1HMZ7T

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

N464578017001 followed by a unit qualifier and the quantity

Package 64578-0170-01. 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 Jul 15, 2025.

Indications (excerpt from the label)

Uses Temporary relief of female concerns: cramps, mood changes, hot flashes.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)