Potassium Chloride Extended-release NDC 71335-1896

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, Extended release

Route

Oral

Labeler

Bryant Ranch Prepack

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 71335-1896_2f7ac23a-6f65-43f4-9b1e-20b2516e2c3aSPL ID 2f7ac23a-6f65-43f4-9b1e-20b2516e2c3aSPL set ID 7b8e7a4f-0d44-46b2-9565-7b4c294e9fcbRxCUI 1801294UNII 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

N471335189601 followed by a unit qualifier and the quantity Copy

Package 71335-1896-01. 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

Other NDCs under ANDA 214452

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