Anxiovita NDC 66343-082

NDC codes

FDA NDC Directory

Product NDC (as listed)66343-082Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66343-0082Add 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
66343-082-60	66343008260	59 mL in 1 BOTTLE (66343-082-60)Marketed from Nov 28, 2022

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Anxiovita
Generic name (nonproprietary): aconitum napellus, anacardium orientale, cerebrum, hypericum perforatum
Active ingredients: Aconitum napellus — 18 [hp_M]/59mLSemecarpus anacardium juice — 12 [hp_X]/59mLSus scrofa cerebrum — 200 [hp_C]/59mLHypericum perforatum — 21 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: RUBIMED AG
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 28, 2022
Listing expires: Dec 31, 2026
Identifiers: Product ID 66343-082_2816f87f-0405-eba7-e063-6394a90ab393SPL ID 2816f87f-0405-eba7-e063-6394a90ab393SPL set ID 258c677b-1a0a-4315-ba0c-4d9892f0534dUNII U0NQ8555JD, Y0F0BU8RDU, 4GB5DQR532, XK4IUX8MNB

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

N466343008260 followed by a unit qualifier and the quantity

Package 66343-0082-60. 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)

Uses: (✝) Homeopathic remedy to alleviate feeling frightened.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)