NDC codes

FDA NDC Directory
Product NDC (as listed)63629-1073Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63629-1073Add 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
63629-1073-1636291073011000 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1073-1)Marketed from Nov 20, 2019

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 Extended-Release
Generic name (nonproprietary)
potassium chloride
Active ingredients
Potassium chloride — 750 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076368
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 63629-1073_a6c64d55-7b11-44a3-9499-b5aa645d56b9SPL ID a6c64d55-7b11-44a3-9499-b5aa645d56b9SPL set ID 80dd5de2-5066-472b-b1f8-88070a5c7388RxCUI 1801298UNII 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

N463629107301 followed by a unit qualifier and the quantity

Package 63629-1073-01. 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)

INDICATIONS AND USAGE BECAUSE OF REPORTS OF INTESTINAL AND GASTRIC ULCERATION AND BLEEDING WITH CONTROLLED RELEASE POTASSIUM CHLORIDE PREPARATIONS, THESE DRUGS SHOULD BE RESERVED FOR THOSE PATIENTS WHO CANNOT TOLERATE OR REFUSE TO TAKE LIQUID OR EFFERVESCENT POTASSIUM PREPARATIONS OR FOR PATIENTS IN WHOM THERE IS A PROBLEM OF COMPLIANCE WITH THESE PREPARATIONS. 1. For the treatment of patients with hypokalemia with or without metabolic alkalosis, in digitalis intoxication, and in patients with hypokalemic familial periodic paralysis. If hypokalemia is the result of diuretic therapy, consideration should be given to the use of a lower dose of diuretic, which may be sufficient without leading …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076368

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

FDA NDC Directory listings under ANDA 076368
ProductStrengthForm · routeLabelerProduct NDC
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-2607
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-3024
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-2866
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralBryant Ranch Prepack63629-1075
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralBryant Ranch Prepack63629-1072
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralBryant Ranch Prepack63629-1074
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralBryant Ranch Prepack72162-1786
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralSun Pharmaceutical Industries, Inc.63304-076
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-2913
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralAmerican Health Packaging60687-632
Potassium ChloridePotassium chloride 20 meq/1Tablet, Extended releaseOralPD-Rx Pharmaceuticals, Inc.72789-365
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-1900
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-2958
Potassium ChloridePotassium chloride 20 meq/1Tablet, Extended releaseOralSun Pharmaceutical Industries, Inc.63304-987
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralMajor Pharmaceuticals0904-7547
Potassium ChloridePotassium chloride 20 meq/1Tablet, Extended releaseOralMajor Pharmaceuticals0904-7548

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