What is NDC 59469-032?

59469-032 is the product NDC for Okoubaka (okoubaka aubrevillei bark), Okoubaka aubrevillei bark 2 [hp_X]/50mL solution/ drops, listed with the FDA by PEKANA Natuheilmittel GmbH. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Okoubaka (Okoubaka aubrevillei Bark).

PEKANA Natuheilmittel GmbH, NDC labeler code 59469. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Okoubaka?

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.

Okoubaka NDC 59469-032 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-032Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0032Add 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
59469-032-10	5946900321059469003210	1 BOTTLE, GLASS in 1 BOX (59469-032-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Apr 12, 2008

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): Okoubaka
Generic name (nonproprietary): okoubaka aubrevillei bark
Active ingredients: Okoubaka aubrevillei bark — 2 [hp_X]/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Natuheilmittel GmbHNDC labeler code 59469
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 12, 2008
Listing expires: Dec 31, 2026
Identifiers: Product ID 59469-032_e3b50a80-d21e-4899-a4c4-50fea6d83bb2SPL ID e3b50a80-d21e-4899-a4c4-50fea6d83bb2SPL set ID baeeb7ce-ab37-4a63-a825-66889a2df30fUNII MK2074187Z

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

N459469003210 followed by a unit qualifier and the quantity

Package 59469-0032-10. 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 Dec 21, 2022.

Indications (excerpt from the label)

Indications For relief of occasional diarrhea. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59469-032

What is NDC 59469-032?: 59469-032 is the product NDC for Okoubaka (okoubaka aubrevillei bark), Okoubaka aubrevillei bark 2 [hp_X]/50mL solution/ drops, listed with the FDA by PEKANA Natuheilmittel GmbH. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Okoubaka (Okoubaka aubrevillei Bark).
What is the active ingredient?: Okoubaka aubrevillei bark.
Who is the labeler?: PEKANA Natuheilmittel GmbH, NDC labeler code 59469. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Okoubaka?: 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.

Okoubaka (Okoubaka aubrevillei bark) NDC 59469-032