Kali bromatum (potassium bromide) NDC 0220-2819

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-2819Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-2819Add 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
0220-2819-41	00220281941	6 [hp_C] in 1 TUBE (0220-2819-41)Marketed from Mar 3, 1983

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Kali bromatum
Generic name (nonproprietary): potassium bromide
Active ingredients: Potassium bromide — 6 [hp_C]/6[hp_C]
Dosage form: Pellet
Route: Oral
Labeler: Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 3, 1983
Listing expires: Dec 31, 2026
Identifiers: Product ID 0220-2819_0a0e1d88-7fbd-8d1d-e063-6394a90a6398SPL ID 0a0e1d88-7fbd-8d1d-e063-6394a90a6398SPL set ID 85169b9d-441e-eb4a-e053-2991aa0abd8eUNII OSD78555ZM

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

N400220281941 followed by a unit qualifier and the quantity

Package 00220-2819-41. 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

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