Anacardium Orientale NDC 63545-971

NDC codes

FDA NDC Directory

Product NDC (as listed)63545-971Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63545-0971Add 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
63545-971-01	63545097101	200 PELLET in 1 VIAL, GLASS (63545-971-01)Marketed from Nov 10, 2020
63545-971-02	63545097102	1200 PELLET in 1 BOTTLE, GLASS (63545-971-02)Marketed from Nov 10, 2020
63545-971-03	63545097103	4000 PELLET in 1 BOTTLE, GLASS (63545-971-03)Marketed from Nov 10, 2020

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): Anacardium Orientale
Generic name (nonproprietary): anacardium orientale
Active ingredients: Semecarpus anacardium juice — 6 [hp_C]/1
Dosage form: Pellet
Route: Oral
Labeler: Hahnemann Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 10, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 63545-971_2b4ab488-302f-9255-e063-6294a90aa870SPL ID 2b4ab488-302f-9255-e063-6294a90aa870SPL set ID b3c68d20-f115-1801-e053-2995a90a5fcfUNII Y0F0BU8RDU

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

N463545097101 followed by a unit qualifier and the quantity

Package 63545-0971-01. 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 Jan 9, 2025.

Full label on DailyMed (opens in a new tab)