Potassium Chloride Extended-Release NDC 60687-632

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

Labeler

American Health Packaging

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 076368

Marketing start

Mar 2, 2023

Listing expires

Dec 31, 2026

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 60687-632_204bc844-c945-938e-e063-6294a90ad011SPL ID 204bc844-c945-938e-e063-6294a90ad011SPL set ID 8c12c5f8-5950-44e3-9473-a0b95187b43cRxCUI 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

N460687063201 followed by a unit qualifier and the quantity Copy

Package 60687-0632-01. 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

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

Other NDCs under ANDA 076368

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