Potassium Chloride NDC 60760-423

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

Labeler

St. Mary's Medical Park Pharmacy

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 209314

Marketing start

Jun 19, 2026

Listing expires

Dec 31, 2027

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 60760-423_549c9d2f-69a6-4019-e063-6294a90a4c43SPL ID 549c9d2f-69a6-4019-e063-6294a90a4c43SPL set ID 549c9d28-bf8b-2dc2-e063-6294a90abe7bRxCUI 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

N460760042390 followed by a unit qualifier and the quantity Copy

Package 60760-0423-90. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 209314

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