Neuropar NDC 44911-0251

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0251Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0251Add 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
44911-0251-1	44911025101	30 mL in 1 BOTTLE, DROPPER (44911-0251-1)Marketed from Aug 31, 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): Neuropar
Generic name (nonproprietary): passiflora incarnata, glandula suprarenalis suis, thyroidinum (bovine), aranea diadema, arnica montana, arsenicum album, hypericum perforatum, lachesis mutus, physostigma venenosum, zincum picricum
Active ingredients: Passiflora incarnata flowering top — 3 [hp_X]/mLSus scrofa adrenal gland — 6 [hp_X]/mLThyroid, Bovine — 6 [hp_X]/mLAraneus diadematus — 12 [hp_X]/mLArnica montana whole — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLHypericum perforatum whole — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLPhysostigma venenosum seed — 15 [hp_X]/mLZinc picrate nonahydrate — 15 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 31, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Copper Ion Absorption (Physiologic effect)
Identifiers: Product ID 44911-0251_cdb53b5c-1fc6-426e-82e7-bbaf3f1b1598SPL ID cdb53b5c-1fc6-426e-82e7-bbaf3f1b1598SPL set ID 76fc7c3d-c001-4ba0-821b-7d8544f6670bUNII CLF5YFS11O, 398IYQ16YV, MN18OTN73W, 6T6CO7R3Z5, O80TY208ZW, S7V92P67HO, XK4IUX8MNB, VSW71SS07I, CJV9E9IIOA, 0057VRD75NUPC 0363113701050
Pharmacologic class: Copper Absorption 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

N444911025101 followed by a unit qualifier and the quantity

Package 44911-0251-01. 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 Oct 29, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve numbness and tingling, stiffness in nape of the neck with shooting pain, and tingling and burning pain with numbness.** **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)