NDC codes

FDA NDC Directory
Product NDC (as listed)75834-280Labeler and product segments. Claims need a package NDC.
Product NDC at billing width75834-0280Add 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
75834-280-087583402800875834028008237 mL in 1 BOTTLE (75834-280-08)Marketed from Dec 29, 2021
75834-280-30758340280307583402803030 mL in 1 BOTTLE, WITH APPLICATOR (75834-280-30)Marketed from Dec 29, 2021

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)
Potassium Iodide
Generic name (nonproprietary)
potassium iodide
Active ingredients
Potassium iodide — 1 g/mL
Dosage form
Solution
Route
Oral
Labeler
Nivagen Pharmaceuticals, Inc.NDC labeler code 75834
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 75834-280_62e50e38-f41a-4dc9-96e8-37a7c677bec5SPL ID 62e50e38-f41a-4dc9-96e8-37a7c677bec5SPL set ID b0bf9487-45d0-4fbc-a8dd-90f505355d14RxCUI 312541UNII 1C4QK22F9JUPC 0375834280080, 0375834280301

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

N475834028008 followed by a unit qualifier and the quantity

Package 75834-0280-08. 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 & USAGE Potassium iodide oral solution, USP is for use as an expectorant in the symptomatic treatment of chronic pulmonary diseases where tenacious mucus complicates the problem, including bronchial asthma, bronchitis and pulmonary emphysema.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 75834-280

What is NDC 75834-280?
75834-280 is the product NDC for Potassium Iodide, Potassium iodide 1 g/mL solution, listed with the FDA by Nivagen Pharmaceuticals, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Potassium Iodide.
What is the active ingredient?
Potassium iodide.
Who is the labeler?
Nivagen Pharmaceuticals, Inc., NDC labeler code 75834. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Potassium Iodide?
2 other product NDCs are listed under this name. See all Potassium Iodide NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Potassium Iodide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Potassium IodidePotassium iodide 1 g/mLSolutionOralBryant Ranch Prepack72162-242372162-2423-0272162-2423-03
Potassium IodidePotassium iodide 65 mg/mLSolutionOralMission Pharmacal Company0178-031400178-0314-30

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