Potassium Chloride Extended-release NDC 68001-567

Product information

Brand name (proprietary)

Potassium Chloride Extended-release

Generic name (nonproprietary)

potassium chloride extended-release

Active ingredients

Potassium chloride — 1500 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Bluepoint Laboratories

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 214452

Marketing start

Jan 30, 2021

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 68001-567_4341146a-910b-db91-e063-6394a90af245SPL ID 4341146a-910b-db91-e063-6394a90af245SPL set ID d605ca36-2bfa-42cb-a46c-8ecb3162994eRxCUI 1801294, 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

N468001056700 followed by a unit qualifier and the quantity Copy

Package 68001-0567-00. 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 214452

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