Bronchi-Pertu NDC 59469-303

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-303Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0303Add 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
59469-303-50	59469030350	1 BOTTLE, GLASS in 1 BOX (59469-303-50) / 250 mL in 1 BOTTLE, GLASSMarketed from Feb 3, 2020

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): Bronchi-Pertu
Generic name (nonproprietary): bryonia dioica root, protortonia cacti, guaiacum officinale resin, oenanthe aquatica fruit, phosphorus, antimony potassium tartrate, usnea barbata, and grindelia hirsutula whole
Active ingredients: Bryonia dioica root — 3 [hp_X]/125mLProtortonia cacti — 2 [hp_X]/125mLGuaiacum officinale resin — 3 [hp_X]/125mLOenanthe aquatica fruit — 4 [hp_X]/125mLPhosphorus — 6 [hp_X]/125mLAntimony potassium tartrate — 6 [hp_X]/125mLUsnea barbata — 12 [hp_X]/125mLGrindelia hirsutula whole — 8 [hp_X]/125mL
Dosage form: Syrup
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
Identifiers: Product ID 59469-303_815b9de3-2368-4bf3-9294-1e3dbb13cf41SPL ID 815b9de3-2368-4bf3-9294-1e3dbb13cf41SPL set ID 6812a35d-4f1b-45c2-a893-a345924af03fUNII 53UB5FH7CX, LZB7TFX1LT, N0K2Z502R6, N4LEE4Z93J, 27YLU75U4W, DL6OZ476V3, D6DVA9TCAP, C08B09D8UJ

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

N459469030350 followed by a unit qualifier and the quantity

Package 59469-0303-50. 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 23, 2022.

Indications (excerpt from the label)

Indications Antitussive expextorant. 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)