Osteopar NDC 44911-0367

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0367Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0367Add 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
44911-0367-1	44911036701	30 mL in 1 BOTTLE, DROPPER (44911-0367-1)Marketed from Jun 16, 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): Osteopar
Generic name (nonproprietary): equisetum hyemale, symphytum officinale, calcarea carbonica, calcarea fluorica, calcarea phosphorica, medulla ossis suis, ossa sepia, silicea, hekla lava
Active ingredients: Equisetum hyemale whole — 3 [hp_X]/mLComfrey root — 6 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLCalcium fluoride — 12 [hp_X]/mLTribasic calcium phosphate — 12 [hp_X]/mLSus scrofa bone marrow — 12 [hp_X]/mLSepia esculenta bone — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLHekla lava — 15 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 16, 2016
Marketing end: Sep 13, 2027
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 44911-0367_e4edf638-e46c-433b-bb5a-d664dd45c560SPL ID e4edf638-e46c-433b-bb5a-d664dd45c560SPL set ID daf83dbf-bbf4-49e2-ade1-1d86f3e52675UNII 59677RXH25, M9VVZ08EKQ, 2E32821G6I, O3B55K4YKI, 91D9GV0Z28, VP2CN2G7Y8, M6XU683549, ETJ7Z6XBU4, C21158IIRKUPC 0363113701081
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

N444911036701 followed by a unit qualifier and the quantity

Package 44911-0367-01. 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 May 9, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve pain in lower back with burning, soreness in the sacroiliac area, and pain in the joints 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)