NDC codes

FDA NDC Directory
Product NDC (as listed)71740-112Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71740-0112Add 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
71740-112-3071740011230717400112301 BOTTLE, WITH APPLICATOR in 1 CARTON (71740-112-30) / 30 mL in 1 BOTTLE, WITH APPLICATORMarketed from Nov 13, 2017

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)
Sski
Generic name (nonproprietary)
potassium iodide
Active ingredients
Potassium iodide — 1 g/mL
Dosage form
Solution
Route
Oral
Labeler
Avondale Pharmaceuticals, LLCNDC labeler code 71740
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 71740-112_6a232f5f-b029-4908-98b1-eda6ab98f451SPL ID 6a232f5f-b029-4908-98b1-eda6ab98f451SPL set ID ca1d3449-ea29-49a4-8863-365ec95f1553RxCUI 312541, 544597UNII 1C4QK22F9JUPC 0371740112309

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

N471740011230 followed by a unit qualifier and the quantity

Package 71740-0112-30. 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)

Indications and Usage SSKI ® (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 71740-112

What is NDC 71740-112?
71740-112 is the product NDC for Sski (potassium iodide), Potassium iodide 1 g/mL solution, listed with the FDA by Avondale Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sski (Potassium Iodide).
What is the active ingredient?
Potassium iodide.
Who is the labeler?
Avondale Pharmaceuticals, LLC, NDC labeler code 71740. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sski?
1 other product NDC are listed under this name. See all Sski 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 Sski NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Sskipotassium iodidePotassium iodide 1 g/mLSolutionOralATLANTIC BIOLOGICALS CORP.17856-011417856-0114-0117856-0114-02

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