Potassium Chloride Extended-Release NDC 71335-2607

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2607Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2607Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package
71335-2607-1	71335260701	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2607-1)Marketed from Mar 11, 2026
71335-2607-2	71335260702	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2607-2)Marketed from Mar 11, 2026
71335-2607-3	71335260703	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2607-3)Marketed from Mar 11, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

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, 2027
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 71335-2607_a70902e1-7c29-427d-ab79-be042819cbf7SPL ID a70902e1-7c29-427d-ab79-be042819cbf7SPL set ID ff44dcd5-b255-4d80-83ee-3c8f922c99ebRxCUI 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

N471335260701 followed by a unit qualifier and the quantity

Package 71335-2607-01. 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

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