NDC codes

FDA NDC Directory
Product NDC (as listed)0603-1554Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00603-1554Add 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
0603-1554-040060315540400603155404100 POUCH in 1 CARTON (0603-1554-04) / 1.58 g in 1 POUCH (0603-1554-10)Marketed from Sep 18, 2015
0603-1554-16006031554160060315541630 POUCH in 1 CARTON (0603-1554-16) / 1.58 g in 1 POUCH (0603-1554-10)Marketed from Sep 18, 2015

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 Chloride
Generic name (nonproprietary)
potassium chloride
Active ingredients
Potassium chloride — 1.5 g/1.58g
Dosage form
Powder, For solution
Route
Oral
Labeler
Endo USA, Inc.NDC labeler code 0603
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 208019
Marketing start
Listing expires
Identifiers
Product ID 0603-1554_05260a26-2484-4fd1-9ca1-8445f239923eSPL ID 05260a26-2484-4fd1-9ca1-8445f239923eSPL set ID a64d7151-09a6-474c-83fc-36c7cf582d32RxCUI 1867544UNII 660YQ98I10

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

N400603155404 followed by a unit qualifier and the quantity

Package 00603-1554-04. 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)

Potassium Chloride is indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in patients for whom dietary management with potassium-rich foods or diuretic dose reduction is insufficient. Potassium Chloride is a potassium salt indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in patients for whom dietary management with potassium-rich foods or diuretic dose reduction is insufficient. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0603-1554

What is NDC 0603-1554?
0603-1554 is the product NDC for Potassium Chloride, Potassium chloride 1.5 g/1.58g powder, for solution, listed with the FDA by Endo USA, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Potassium Chloride.
What is the active ingredient?
Potassium chloride.
Who is the labeler?
Endo USA, Inc., NDC labeler code 0603. 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 Chloride?
216 other product NDCs are listed under this name. See all Potassium Chloride 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 Chloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Potassium Chloridepotassium chloride oralPotassium chloride 1.5 g/15mLSolutionOralCardinal Health 107, LLC55154-802655154-8026-05
Potassium ChloridePotassium chloride 1.5 g/1.58gPowder, For solutionOralCardinal Health 107, LLC55154-835255154-8352-05
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralCoupler LLC67046-103267046-1032-03
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralSt. Mary's Medical Park Pharmacy60760-42360760-0423-90
Potassium ChloridePotassium chloride 750 mg/1Tablet, Extended releaseOralNorthwind Health Company, LLC82868-11182868-0111-90
Potassium ChloridePotassium chloride 20 meq/15mLSolutionOralAjenat Pharmaceuticals LLC82983-41182983-0411-47
Potassium ChloridePotassium chloride 40 meq/15mLSolutionOralAjenat Pharmaceuticals LLC82983-41282983-0412-47
Potassium ChloridePotassium chloride 20 meq/1Tablet, Extended releaseOralMajor Pharmaceuticals0904-754800904-7548-61
Potassium ChloridePotassium chloride 3 g/3.16gFor solutionOralIPG Pharmaceuticals, Inc.71085-08371085-0083-30
Potassium ChloridePotassium chloride 20 meq/15mLSolutionOralAurobindo Pharma Limited59651-95959651-0959-47

All 217 Potassium Chloride NDCs

Other NDCs under NDA 208019

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under NDA 208019
ProductStrengthForm · routeLabelerProduct NDC
Pokonzapotassium chloridePotassium chloride .75 g/.79gPowder, For solutionOralCarwin Pharmaceutical Associates, LLC15370-305
Pokonzapotassium chloridePotassium chloride 1.125 g/1.185gPowder, For solutionOralCarwin Pharmaceutical Associates, LLC15370-306
Potassium ChloridePotassium chloride 1.5 g/1.58gPowder, For solutionOralGenus Lifesciences Inc.64950-321
Potassium ChloridePotassium chloride 3 g/3.16gFor solutionOralIPG Pharmaceuticals, Inc.71085-083

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