Potassium Chloride Extended-Release NDC 72162-1786

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

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

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

Marketing start

Nov 20, 2019

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 72162-1786_000215d5-841c-4f90-bfd4-de560e5e042aSPL ID 000215d5-841c-4f90-bfd4-de560e5e042aSPL set ID 863e6980-4a66-48a5-a14f-828a00480c93RxCUI 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

N472162178600 followed by a unit qualifier and the quantity Copy

Package 72162-1786-00. 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

Other NDCs under ANDA 076368

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