apo-STRUM NDC 59469-323

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-323Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0323Add 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
59469-323-10	59469032310	1 BOTTLE, GLASS in 1 BOX (59469-323-10) / 50 mL in 1 BOTTLE, GLASSMarketed 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): apo-STRUM
Generic name (nonproprietary): calcium fluoride, conium maculatum flowering top, lophophytum leandrii, hedera helix flowering twig, magnesium carbonate, cytisus scoparius flowering top, selenicereus grandiflorus whole, and galium aparine
Active ingredients: Calcium fluoride — 8 [hp_X]/50mLConium maculatum flowering top — 6 [hp_X]/50mLLophophytum leandrii — 4 [hp_X]/50mLHedera helix flowering twig — 3 [hp_X]/50mLMagnesium carbonate — 8 [hp_X]/50mLCytisus scoparius flowering top — 6 [hp_X]/50mLSelenicereus grandiflorus whole — 4 [hp_X]/50mLGalium aparine whole — 584 mg/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel GmbH
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 24, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 59469-323_f9f8ce45-cc62-4715-876e-b4d38c2cc32fSPL ID f9f8ce45-cc62-4715-876e-b4d38c2cc32fSPL set ID 9b4874fc-bb67-4627-8096-acedaeb81592UNII O3B55K4YKI, Q28R5GF371, 59150S2EOG, 3D10KUA6BM, 0E53J927NA, XZC6H8R666, X8H7HS7MRM, Z4B6561488
Pharmacologic class: Non-Standardized Plant Allergenic Extract

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

N459469032310 followed by a unit qualifier and the quantity

Package 59469-0323-10. 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 Jan 11, 2023.

Indications (excerpt from the label)

Indications Regulative drops. 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)