Hypothalmupar NDC 44911-0473

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0473Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0473Add 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
44911-0473-1	44911047301	30 mL in 1 BOTTLE, DROPPER (44911-0473-1)Marketed from Sep 24, 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): Hypothalmupar
Generic name (nonproprietary): aralia quinquefolia, ginkgo biloba, hydrocotyle asiatica, cerebrum suis, hypophysis suis, hypothalamus suis, phosphorus, silicea
Active ingredients: American ginseng — 3 [hp_X]/mLGinkgo — 3 [hp_X]/mLCentella asiatica whole — 3 [hp_X]/mLSus scrofa cerebrum — 8 [hp_X]/mLSus scrofa pituitary gland — 8 [hp_X]/mLSus scrofa hypothalamus — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 24, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0473_e646941c-406d-4e3e-af16-bcd09d44ea78SPL ID e646941c-406d-4e3e-af16-bcd09d44ea78SPL set ID 8b01e718-83b7-4f93-8fea-d0e37c756185UNII 8W75VCV53Q, 19FUJ2C58T, 7M867G6T1U, 4GB5DQR532, L0PFEMQ1DT, N6R0856Z79, 27YLU75U4W, ETJ7Z6XBU4UPC 0363113700220

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

N444911047301 followed by a unit qualifier and the quantity

Package 44911-0473-01. 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 28, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve weakness, exhaustion, dizziness, and difficult mental concentration.** **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)