NDC codes

FDA NDC Directory
Product NDC (as listed)61480-255Labeler and product segments. Claims need a package NDC.
Product NDC at billing width61480-0255Add 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 NDC11-digit (billing)PackageCopy
61480-255-05614800255056148002550590 TABLET in 1 BOTTLE (61480-255-05)Marketed from Nov 15, 2001

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 Forte
Generic name (nonproprietary)
nickel sulfate, potassium bromide, and fumaric acid
Active ingredients
Nickel sulfate — 1 [hp_X]/1Potassium bromide — 1 [hp_X]/1Fumaric acid — 1 [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
Listing expires
Identifiers
Product ID 61480-255_440c889d-1e85-767e-e063-6394a90abaa8SPL ID 440c889d-1e85-767e-e063-6394a90abaa8SPL set ID 7896794a-60bd-4dfa-abfe-aa29aaa6f74dUNII 4FLT4T3WUN, OSD78555ZM, 88XHZ13131

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

N461480025505 followed by a unit qualifier and the quantity

Package 61480-0255-05. 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 .

Indications (excerpt from the label)

INDICATIONS PSORIZIDE ® Forte is indicated for the treatment of contact dermatitis due to nickel (metal/jewelry allergy,) dyshidrotic hand/foot eczema, and mild to severe psoriasis. It has been found to work well with a variety of combination therapies. Eczema, seborrhea and a variety of chronic pruritic inflammatory dermatoses generally respond well also.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 61480-255

What is NDC 61480-255?
61480-255 is the product NDC for Psorizide Forte, Nickel sulfate 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 Forte (Nickel Sulfate, Potassium Bromide, and Fumaric Acid).
What is the active ingredient?
Nickel sulfate, Potassium bromide, Fumaric acid.
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 Forte?
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.

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