What is NDC 59469-140?

59469-140 is the product NDC for Mundipur, Bryonia dioica root 4 [hp_X]/250mL + 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?

Mundipur (Bryonia Dioica Root, Colchicum autumnale Bulb, Sodium Carbonate, Phytolacca americana Root, Berberis Vulgaris Root Bark, Cynara scolymus Whole, Harpagophytum procumbens Root, and Ledum Palustre Twig).

What is the active ingredient?

Bryonia dioica root, Colchicum autumnale bulb, Sodium carbonate, Phytolacca americana root, Berberis vulgaris root bark, Cynara scolymus whole, Harpagophytum procumbens root, Rhododendron tomentosum leafy twig.

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 Mundipur?

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.

Mundipur NDC 59469-140 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-140Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0140Add 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
59469-140-50	5946901405059469014050	1 BOTTLE, GLASS in 1 BOX (59469-140-50) / 250 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): Mundipur
Generic name (nonproprietary): bryonia dioica root, colchicum autumnale bulb, sodium carbonate, phytolacca americana root, berberis vulgaris root bark, cynara scolymus whole, harpagophytum procumbens root, and ledum palustre twig
Active ingredients: Bryonia dioica root — 4 [hp_X]/250mLColchicum autumnale bulb — 12 [hp_X]/250mLSodium carbonate — 4 [hp_X]/250mLPhytolacca americana root — 4 [hp_X]/250mLBerberis vulgaris root bark — 6 [hp_X]/250mLCynara scolymus whole — 8 [hp_X]/250mLHarpagophytum procumbens root — 12 [hp_X]/250mLRhododendron tomentosum leafy twig — 6 [hp_X]/250mL
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: Apr 12, 2008
Listing expires: Dec 31, 2026
Identifiers: Product ID 59469-140_fb347aec-4719-4086-9abd-1c79936b818fSPL ID fb347aec-4719-4086-9abd-1c79936b818fSPL set ID 4aeba0c8-0d53-4012-8024-df1e82585cb3UNII 53UB5FH7CX, 993QHL78E6, 45P3261C7T, 11E6VI8VEG, 1TH8Q20J0U, 9N3437ZUU0, 1OYM338E89, 877L01IZ0P

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

N459469014050 followed by a unit qualifier and the quantity

Package 59469-0140-50. 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 16, 2022.

Indications (excerpt from the label)

Indications For relief of occasional minor rheumatic symptoms such as stiffness and joint 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 59469-140

What is NDC 59469-140?: 59469-140 is the product NDC for Mundipur, Bryonia dioica root 4 [hp_X]/250mL + 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?: Mundipur (Bryonia Dioica Root, Colchicum autumnale Bulb, Sodium Carbonate, Phytolacca americana Root, Berberis Vulgaris Root Bark, Cynara scolymus Whole, Harpagophytum procumbens Root, and Ledum Palustre Twig).
What is the active ingredient?: Bryonia dioica root, Colchicum autumnale bulb, Sodium carbonate, Phytolacca americana root, Berberis vulgaris root bark, Cynara scolymus whole, Harpagophytum procumbens root, Rhododendron tomentosum leafy twig.
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 Mundipur?: 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.