What is NDC 80353-551?

80353-551 is the product NDC for Archibone, Achyranthes japonica root 1 [hp_X]/1; Prunus persica whole 1 [hp_X]/1 capsule, listed with the FDA by HCBIOPHARM LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Archibone (Rheumatoid arthritis and osteoarthritis recovery, and cartilage restore).

What is the active ingredient?

Achyranthes japonica root, Prunus persica whole.

HCBIOPHARM LLC, NDC labeler code 80353. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Archibone?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Archibone NDC 80353-551 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)80353-551Labeler and product segments. Claims need a package NDC.

Product NDC at billing width80353-0551Add 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
80353-551-01	80353055101	1 BOTTLE in 1 BOX (80353-551-01) / 1 CAPSULE in 1 BOTTLE (80353-551-02) / 60 CAPSULE in 1 CAPSULE (80353-551-03)Marketed from Nov 19, 2021

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): Archibone
Generic name (nonproprietary): rheumatoid arthritis and osteoarthritis recovery, and cartilage restore
Active ingredients: Achyranthes japonica root — 1 [hp_X]/1Prunus persica whole — 1 [hp_X]/1
Dosage form: Capsule
Route: Oral
Labeler: HCBIOPHARM LLCNDC labeler code 80353
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 19, 2021
Listing expires: Dec 31, 2027
Identifiers: Product ID 80353-551_4e3b30cf-8f56-5e35-e063-6294a90a2383SPL ID 4e3b30cf-8f56-5e35-e063-6294a90a2383SPL set ID d0a28ea1-46a4-cdcf-e053-2a95a90a0e8bUNII IM19VOE23G, 4E7YW35Q0H

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

N480353055101 followed by a unit qualifier and the quantity

Package 80353-0551-01. 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 Mar 30, 2026.

Indications (excerpt from the label)

Use To reverse rheumatoid arthritis To reverse osteoarthritis To rebuild cartilage To relieve joint pain

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 80353-551

What is NDC 80353-551?: 80353-551 is the product NDC for Archibone, Achyranthes japonica root 1 [hp_X]/1; Prunus persica whole 1 [hp_X]/1 capsule, listed with the FDA by HCBIOPHARM LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Archibone (Rheumatoid arthritis and osteoarthritis recovery, and cartilage restore).
What is the active ingredient?: Achyranthes japonica root, Prunus persica whole.
Who is the labeler?: HCBIOPHARM LLC, NDC labeler code 80353. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Archibone?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.