NDC codes

FDA NDC Directory
Product NDC (as listed)50090-5335Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-5335Add 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
50090-5335-05009053350030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-0)Marketed from Nov 4, 2020
50090-5335-150090533501100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-1)Marketed from Nov 4, 2020
50090-5335-25009053350290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-2)Marketed from Nov 4, 2020
50090-5335-35009053350360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5335-3)Marketed from Nov 4, 2020

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 750 mg/1
Dosage form
Tablet, Film coated, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210921
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 50090-5335_dbf5cc65-196b-4d7c-a311-d30c7d9fef63SPL ID dbf5cc65-196b-4d7c-a311-d30c7d9fef63SPL set ID e1670127-c551-441b-bac4-39f10a6d156fRxCUI 628953UNII 660YQ98I10
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

N450090533500 followed by a unit qualifier and the quantity

Package 50090-5335-00. 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 extended-release tablets are 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 extended-release tablets are 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)

Other NDCs under ANDA 210921

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

FDA NDC Directory listings under ANDA 210921
ProductStrengthForm · routeLabelerProduct NDC
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralREMEDYREPACK INC.70518-2964
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralBluePoint Laboratories68001-518
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralMajor Pharmaceuticals0904-7216
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralPreferred Pharmaceuticals Inc.68788-8262
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralCoupler LLC67046-1032
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralAphena Pharma Solutions - Tennessee, LLC71610-944
Potassium ChloridePotassium chloride 600 mg/1Tablet, Film coated, Extended releaseOralAurobindo Pharma Limited65862-986
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralAurobindo Pharma Limited65862-987
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralAmerican Health Packaging60687-810
Potassium ChloridePotassium chloride 600 mg/1Tablet, Film coated, Extended releaseOralBryant Ranch Prepack63629-2620
Potassium ChloridePotassium chloride 750 mg/1Tablet, Film coated, Extended releaseOralNorthwind Health Company, LLC51655-463

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