What is NDC 61480-124?

61480-124 is the product NDC for Psorizide Ultra, Potassium bromide 1 [hp_X]/1 + 2 more ingredients tablet, listed with the FDA by PLYMOUTH HEALTHCARE PRODUCTS LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Psorizide Ultra (Potassium Bromide, Nickel Sulfate, and Zinc Bromide).

What is the active ingredient?

Potassium bromide, Nickel sulfate, Zinc bromide.

PLYMOUTH HEALTHCARE PRODUCTS LLC, NDC labeler code 61480. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Psorizide Ultra?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Psorizide Ultra NDC 61480-124 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)61480-124Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61480-0124Add 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
61480-124-05	6148001240561480012405	100 TABLET in 1 BOTTLE (61480-124-05)Marketed from Oct 1, 1997

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): Psorizide Ultra
Generic name (nonproprietary): potassium bromide, nickel sulfate, and zinc bromide
Active ingredients: Potassium bromide — 1 [hp_X]/1Nickel sulfate — 1 [hp_X]/1Zinc bromide — 4 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: PLYMOUTH HEALTHCARE PRODUCTS LLCNDC labeler code 61480
Product type: Prescription drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 1, 1997
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Copper Ion Absorption (Physiologic effect)
Identifiers: Product ID 61480-124_2b242c2f-68f0-089a-e063-6394a90a405fSPL ID 2b242c2f-68f0-089a-e063-6394a90a405fSPL set ID 78d05c25-6817-4763-b662-6dbb0625fa84UNII OSD78555ZM, 4FLT4T3WUN, OO7ZBU9703UPC 0361480124052
Pharmacologic class: Copper Absorption Inhibitor

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

N461480012405 followed by a unit qualifier and the quantity

Package 61480-0124-05. 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 7, 2025.

Indications (excerpt from the label)

INDICATIONS PSORIZIDE ® ULTRA is indicated for the treatment of moderate to severe eczema, atopic dermatitis, seborrhea and seborrheic dermatitis. It has been found to work well with variety of combination therapies. Psoriasis also responds, but generally has a more favorable response to PSORIZIDE ® Forte (NDC 61480-255-05.)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 61480-124

What is NDC 61480-124?: 61480-124 is the product NDC for Psorizide Ultra, Potassium bromide 1 [hp_X]/1 + 2 more ingredients tablet, listed with the FDA by PLYMOUTH HEALTHCARE PRODUCTS LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Psorizide Ultra (Potassium Bromide, Nickel Sulfate, and Zinc Bromide).
What is the active ingredient?: Potassium bromide, Nickel sulfate, Zinc bromide.
Who is the labeler?: PLYMOUTH HEALTHCARE PRODUCTS LLC, NDC labeler code 61480. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Psorizide Ultra?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.