Potassium Chloride NDC 64380-875

NDC codes

FDA NDC Directory

Product NDC (as listed)64380-875Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64380-0875Add 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
64380-875-68	64380087568	10 POUCH in 1 CARTON (64380-875-68) / 1.58 g in 1 POUCH (64380-875-00)Marketed from Oct 17, 2024
64380-875-69	64380087569	30 POUCH in 1 CARTON (64380-875-69) / 1.58 g in 1 POUCH (64380-875-00)Marketed from Oct 24, 2022
64380-875-70	64380087570	100 POUCH in 1 CARTON (64380-875-70) / 1.58 g in 1 POUCH (64380-875-00)Marketed from Oct 24, 2022

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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
Generic name (nonproprietary): potassium chloride
Active ingredients: Potassium chloride — 1.5 g/1.58g
Dosage form: Powder, For solution
Route: Oral
Labeler: Strides Pharma Science Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211667
Marketing start: Oct 24, 2022
Listing expires: Dec 31, 2027
Identifiers: Product ID 64380-875_4a3559db-aff4-4132-a529-ea3871a3b020SPL ID 4a3559db-aff4-4132-a529-ea3871a3b020SPL set ID f4e36462-3522-4130-8785-6c18871d2984RxCUI 1867544UNII 660YQ98I10UPC 0364380875000

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

N464380087568 followed by a unit qualifier and the quantity

Package 64380-0875-68. 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

Current FDA label (SPL), effective Oct 10, 2025.

Indications (excerpt from the label)

Potassium Chloride is indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in patients for whom dietary management with potassium-rich foods or diuretic dose reduction is insufficient. Potassium chloride is a potassium salt indicated for the treatment and prophylaxis of hypokalemia with or without metabolic alkalosis, in patients for whom dietary management with potassium-rich foods or diuretic dose reduction is insufficient. (1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 211667

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

FDA NDC Directory listings under ANDA 211667
Product	Strength	Form · route	Labeler	Product NDC
Potassium Chloride	Potassium chloride 1.5 g/1.58g	Powder, For solutionOral	Kesin Pharma Corporation	81033-413
Potassium Chloride	Potassium chloride 1.5 g/1.58g	Powder, For solutionOral	American Health Packaging	60687-855
Potassium Chloride	Potassium chloride 1.5 g/1.58g	Powder, For solutionOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-856