What is NDC 0220-3329?

0220-3329 is the product NDC for Medulla Ossis Suis (sus scrofa bone marrow), Sus scrofa bone marrow 8 [hp_X]/8[hp_X] pellet, listed with the FDA by BOIRON. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Medulla Ossis Suis (Sus scrofa bone marrow).

BOIRON, NDC labeler code 0220. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Medulla Ossis Suis?

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.

Medulla Ossis Suis NDC 0220-3329 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-3329Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-3329Add 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
0220-3329-41	00220332941	8 [hp_X] in 1 TUBE (0220-3329-41)Marketed from Jan 8, 2018

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Medulla Ossis Suis
Generic name (nonproprietary): sus scrofa bone marrow
Active ingredients: Sus scrofa bone marrow — 8 [hp_X]/8[hp_X]
Dosage form: Pellet
Route: Oral
Labeler: BOIRONNDC labeler code 0220
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 8, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 0220-3329_0a1f531e-55e6-7573-e063-6294a90aaa48SPL ID 0a1f531e-55e6-7573-e063-6294a90aaa48SPL set ID 61e659a2-f4af-42db-e053-2991aa0ab8f5UNII VP2CN2G7Y8

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

N400220332941 followed by a unit qualifier and the quantity

Package 00220-3329-41. 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 Nov 14, 2023.

Indications (excerpt from the label)

Arthritic pain in spine

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0220-3329

What is NDC 0220-3329?: 0220-3329 is the product NDC for Medulla Ossis Suis (sus scrofa bone marrow), Sus scrofa bone marrow 8 [hp_X]/8[hp_X] pellet, listed with the FDA by BOIRON. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Medulla Ossis Suis (Sus scrofa bone marrow).
What is the active ingredient?: Sus scrofa bone marrow.
Who is the labeler?: BOIRON, NDC labeler code 0220. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Medulla Ossis Suis?: 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.

Medulla Ossis Suis (Sus scrofa bone marrow) NDC 0220-3329