NDC codes

FDA NDC Directory
Product NDC (as listed)0245-5315Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00245-5315Add 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
0245-5315-010024553150100245531501100 BLISTER PACK in 1 BLISTER PACK (0245-5315-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0245-5315-89)Marketed from Jun 21, 2019
0245-5315-110024553151100245531511100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-5315-11)Marketed from Jun 21, 2019
0245-5315-150024553151500245531515500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0245-5315-15)Marketed from Jun 21, 2019

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)
Klor-Con
Generic name (nonproprietary)
potassium chloride
Active ingredients
Potassium chloride — 600 mg/1
Dosage form
Tablet, Film coated, Extended release
Route
Oral
Labeler
Upsher-Smith Laboratories, LLCNDC labeler code 0245
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 019123
Marketing start
Listing expires
Other FDA classes
Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers
Product ID 0245-5315_39e77e07-bdc8-28e9-e063-6394a90a120cSPL ID 39e77e07-bdc8-28e9-e063-6394a90a120cSPL set ID 1ff53330-065c-4213-9c0c-ac498621d09dRxCUI 312529, 628953, 628958, 832718UNII 660YQ98I10UPC 0302455316119, 0302455315112
Pharmacologic class
Osmotic Laxative; Potassium Salt

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

N400245531501 followed by a unit qualifier and the quantity

Package 00245-5315-01. 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)

Klor-Con 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. KLOR-CON 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 0245-5315

What is NDC 0245-5315?
0245-5315 is the product NDC for Klor-Con (potassium chloride), Potassium chloride 600 mg/1 tablet, film coated, extended release, listed with the FDA by Upsher-Smith Laboratories, LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Klor-Con (Potassium chloride).
What is the active ingredient?
Potassium chloride.
Who is the labeler?
Upsher-Smith Laboratories, LLC, NDC labeler code 0245. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Klor-Con?
4 other product NDCs are listed under this name. See all Klor-Con 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 Klor-Con NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Klor-Conpotassium chloridePotassium chloride 600 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC0245-083500245-0835-0100245-0835-1100245-0835-15
Klor-Conpotassium chloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC0245-083600245-0836-0100245-0836-1100245-0836-15
Klor-Conpotassium chloridePotassium chloride 1.5 g/1Powder, For solutionOralUpsher-Smith Laboratories, LLC0245-036000245-0360-0100245-0360-30
Klor-Conpotassium chloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC0245-531600245-5316-0100245-5316-1100245-5316-15

Other NDCs under NDA 019123

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

FDA NDC Directory listings under NDA 019123
ProductStrengthForm · routeLabelerProduct NDC
Klor-Conpotassium chloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC0245-5316
Potassium ChloridePotassium chloride 600 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC0832-5322
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralUpsher-Smith Laboratories, LLC0832-5323
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralAvKARE42291-506
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralA-S Medication Solutions50090-7639
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralA-S Medication Solutions50090-7640
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralNorthwind Health Company, LLC51655-226
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralAphena Pharma Solutions - Tennessee, LLC71610-349

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