What is NDC 59469-130?

59469-130 is the product NDC for apo-DOLOR, Aconitum napellus whole 12 [hp_X]/50mL + 7 more ingredients solution/ drops, listed with the FDA by PEKANA Naturheilmittel GmbH. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

apo-DOLOR (Aconitum Napellus, Semecarpus anacardium Fruit, Bryonia Dioica Root, Gelsemium sempervirens Root, Menyanthes trifoliata, Piper methysticum Root, Schoenocaulon officinale Seed, and Spigelia Anthelmia).

What is the active ingredient?

Aconitum napellus whole, Semecarpus anacardium fruit, Bryonia dioica root, Gelsemium sempervirens root, Menyanthes trifoliata whole, Macropiper methysticum root, Schoenocaulon officinale seed, Spigelia anthelmia whole.

PEKANA Naturheilmittel 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 apo-DOLOR?

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.

apo-DOLOR NDC 59469-130 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-130Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0130Add 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
59469-130-10	5946901301059469013010	1 BOTTLE, GLASS in 1 BOX (59469-130-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Dec 11, 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): apo-DOLOR
Generic name (nonproprietary): aconitum napellus, semecarpus anacardium fruit, bryonia dioica root, gelsemium sempervirens root, menyanthes trifoliata, piper methysticum root, schoenocaulon officinale seed, and spigelia anthelmia
Active ingredients: Aconitum napellus whole — 12 [hp_X]/50mLSemecarpus anacardium fruit — 6 [hp_X]/50mLBryonia dioica root — 3 [hp_X]/50mLGelsemium sempervirens root — 4 [hp_X]/50mLMenyanthes trifoliata whole — 3 [hp_X]/50mLMacropiper methysticum root — 8 [hp_X]/50mLSchoenocaulon officinale seed — 3 [hp_X]/50mLSpigelia anthelmia whole — 3 [hp_X]/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel GmbHNDC labeler code 59469
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 11, 2008
Listing expires: Dec 31, 2026
Identifiers: Product ID 59469-130_7b291567-96a5-4023-91c2-e9cafc019bc1SPL ID 7b291567-96a5-4023-91c2-e9cafc019bc1SPL set ID 748ac14d-4306-48da-bcd4-c2eb6413457dUNII U0NQ8555JD, 7399B063X9, 53UB5FH7CX, 639KR60Q1Q, 7H0QTZ446K, BOW48C81XP, 6NAF1689IO, WYT05213GE

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

N459469013010 followed by a unit qualifier and the quantity

Package 59469-0130-10. 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 2, 2022.

Indications (excerpt from the label)

Indications For relief of minor headaches, and muscle pain. 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 59469-130

What is NDC 59469-130?: 59469-130 is the product NDC for apo-DOLOR, Aconitum napellus whole 12 [hp_X]/50mL + 7 more ingredients solution/ drops, listed with the FDA by PEKANA Naturheilmittel GmbH. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: apo-DOLOR (Aconitum Napellus, Semecarpus anacardium Fruit, Bryonia Dioica Root, Gelsemium sempervirens Root, Menyanthes trifoliata, Piper methysticum Root, Schoenocaulon officinale Seed, and Spigelia Anthelmia).
What is the active ingredient?: Aconitum napellus whole, Semecarpus anacardium fruit, Bryonia dioica root, Gelsemium sempervirens root, Menyanthes trifoliata whole, Macropiper methysticum root, Schoenocaulon officinale seed, Spigelia anthelmia whole.
Who is the labeler?: PEKANA Naturheilmittel 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 apo-DOLOR?: 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.