Potassium Chloride NDC 63304-987

Product information

Brand name (proprietary)

Potassium Chloride

Generic name (nonproprietary)

potassium chloride

Active ingredients

Potassium chloride — 20 meq/1

Dosage form

Tablet, Extended release

Route

Oral

Labeler

Sun Pharmaceutical Industries, Inc.

Product type

Prescription drug

Marketing category

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

Marketing start

Nov 14, 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 63304-987_0a1f3d5d-13ce-97b3-e063-6394a90aa250SPL ID 0a1f3d5d-13ce-97b3-e063-6394a90aa250SPL set ID 0a1f2f64-3b0b-5e5c-e063-6294a90a7185RxCUI 1801294UNII 660YQ98I10UPC 0363304987010

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

N463304098701 followed by a unit qualifier and the quantity Copy

Package 63304-0987-01. 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 076368

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