Potassium Chloride (potassium chloride oral) NDC 60687-884

Product information

Brand name (proprietary)

Potassium Chloride

Generic name (nonproprietary)

potassium chloride oral

Active ingredients

Potassium chloride — 1.5 g/15mL

Dosage form

Solution

Route

Oral

Labeler

American Health Packaging

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 211648

Marketing start

Mar 30, 2025

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 60687-884_5c28168c-6d13-7725-e063-6294a90aba36SPL ID 5c28168c-6d13-7725-e063-6294a90aba36

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

N460687088407 followed by a unit qualifier and the quantity Copy

Package 60687-0884-07. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 211648

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