Ligapar NDC 44911-0477

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0477Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0477Add 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
44911-0477-1	44911047701	30 mL in 1 BOTTLE, DROPPER (44911-0477-1)Marketed from Oct 12, 2018

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): Ligapar
Generic name (nonproprietary): lappa major, ligament (human), cartilago suis, arnica montana, bryonia (alba), calcarea phosphorica, causticum, rhododendron chrysanthum, rhus tox, ruta graveolens, silicea, zincum metallicum
Active ingredients: Arctium lappa root — 3 [hp_X]/mLHuman ligament — 8 [hp_X]/mLSus scrofa cartilage — 8 [hp_X]/mLArnica montana whole — 12 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLTribasic calcium phosphate — 12 [hp_X]/mLCausticum — 12 [hp_X]/mLRhododendron aureum leaf — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLRuta graveolens flowering top — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLZinc — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 12, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 44911-0477_c129ac7a-bc5e-4d72-939b-e77fe189f560SPL ID c129ac7a-bc5e-4d72-939b-e77fe189f560SPL set ID 17f6b1f5-8e49-49df-bad4-9c19fa677e69UNII 597E9BI3Z3, S3Q2347PKA, 73ECW5WG2F, O80TY208ZW, T7J046YI2B, 91D9GV0Z28, DD5FO1WKFU, IV92NQJ73U, 6IO182RP7A, N94C2U587S, ETJ7Z6XBU4, J41CSQ7QDSUPC 0363113700725
Pharmacologic class: Blood Coagulation Factor; Phosphate Binder

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

N444911047701 followed by a unit qualifier and the quantity

Package 44911-0477-01. 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 Apr 22, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve painful lower back with burning, sprains, and general soreness and aching of tendons, ligaments and bones.** **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)