Potassium Chloride NDC 70436-002

Product information

Brand name (proprietary)

Potassium Chloride

Generic name (nonproprietary)

potassium chloride

Active ingredients

Potassium chloride — 750 mg/1

Dosage form

Tablet, Film coated, Extended release

Route

Oral

Labeler

Slate Run Pharmaceuticals, LLC

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 209314

Marketing start

Nov 15, 2018

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 70436-002_3bc24552-db33-312e-e063-6294a90a7efdSPL ID 3bc24552-db33-312e-e063-6294a90a7efdSPL set ID 0cc57ece-f15a-4160-a5ea-8d6fa9f9e754RxCUI 312529, 628953UNII 660YQ98I10UPC 0370436001033, 0370436001019, 0370436002030, 0370436002016

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

N470436000201 followed by a unit qualifier and the quantity Copy

Package 70436-0002-01. 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 209314

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