apo-ENTERIT NDC 59469-158

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-158Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0158Add 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
59469-158-10	59469015810	1 BOTTLE, GLASS in 1 BOX (59469-158-10) / 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): apo-ENTERIT
Generic name (nonproprietary): citrullus colocynthis fruit pulp, podophyllum, veratrum album root, artemisia abrotanum flowering top, cynara scolymus whole, and potentilla anserina flowering top
Active ingredients: Citrullus colocynthis fruit pulp — 4 [hp_X]/50mLPodophyllum — 4 [hp_X]/50mLVeratrum album root — 4 [hp_X]/50mLArtemisia abrotanum flowering top — 760 mg/50mLCynara scolymus whole — 2137 mg/50mLPotentilla anserina flowering top — 1092 mg/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel GmbH
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 12, 2008
Listing expires: Dec 31, 2026
Identifiers: Product ID 59469-158_ea8d652c-1583-4429-9d09-928b215a9275SPL ID ea8d652c-1583-4429-9d09-928b215a9275SPL set ID 0c2efd18-2f1e-4bb3-99e2-b9752db16626UNII 23H32AOH17, 2S713A4VP3, QNS6W5US1Z, QG07G580U0, 9N3437ZUU0, H00Y243SK0

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

N459469015810 followed by a unit qualifier and the quantity

Package 59469-0158-10. 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 occasional diarrhea and minor stomach cramps. 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)