CitriPlus NDC 59469-321

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-321Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0321Add 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
59469-321-40	59469032140	1 BOTTLE, GLASS in 1 BOX (59469-321-40) / 100 mL in 1 BOTTLE, GLASS (59469-321-30)Marketed from Jun 24, 2019

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): CitriPlus
Generic name (nonproprietary): juglans regia whole and anhydrous citric acid
Active ingredients: Juglans regia whole — 5 [hp_X]/100mLAnhydrous citric acid — 4 [hp_X]/100mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Natuheilmittel GmbH
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 24, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)
Identifiers: Product ID 59469-321_33ce0ab6-8bec-468d-9f7c-522779c4827dSPL ID 33ce0ab6-8bec-468d-9f7c-522779c4827dSPL set ID 11db1b5b-2959-42c4-a059-25c951933004UNII 87EJ76IO83, XF417D3PSL
Pharmacologic class: Anti-coagulant; Calculi Dissolution Agent

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

N459469032140 followed by a unit qualifier and the quantity

Package 59469-0321-40. 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 Jan 11, 2023.

Indications (excerpt from the label)

Indications For energy. 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)