NDC codes

FDA NDC Directory
Product NDC (as listed)0178-0314Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00178-0314Add 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
0178-0314-3000178031430001780314301 BOTTLE, DROPPER in 1 CARTON (0178-0314-30) / 30 mL in 1 BOTTLE, DROPPERMarketed from May 15, 2016

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)
Potassium Iodide
Generic name (nonproprietary)
potassium iodide
Active ingredients
Potassium iodide — 65 mg/mL
Dosage form
Solution
Route
Oral
Labeler
Mission Pharmacal CompanyNDC labeler code 0178
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206211
Marketing start
Listing expires
Identifiers
Product ID 0178-0314_47d4999c-1880-6c77-e063-6294a90afa06SPL ID 47d4999c-1880-6c77-e063-6294a90afa06SPL set ID d9e02a48-8129-9076-78b2-db01750bd220RxCUI 242429UNII 1C4QK22F9J

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

N400178031430 followed by a unit qualifier and the quantity

Package 00178-0314-30. 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)

Use Helps prevent radioactive iodine from getting into the thyroid gland during a nuclear radiation emergency. Use along with other emergency measures recommended by public officials.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0178-0314

What is NDC 0178-0314?
0178-0314 is the product NDC for Potassium Iodide, Potassium iodide 65 mg/mL solution, listed with the FDA by Mission Pharmacal Company. It has 1 package NDC, 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?
Mission Pharmacal Company, NDC labeler code 0178. 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 1 g/mLSolutionOralNivagen Pharmaceuticals, Inc.75834-28075834-0280-0875834-0280-30

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