NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1131Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1131Add 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 NDC11-digit (billing)PackageCopy
71335-1131-17133511310130 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-1)Marketed from Mar 5, 2019
71335-1131-27133511310260 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-2)Marketed from Mar 5, 2019
71335-1131-37133511310390 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-3)Marketed from Mar 5, 2019
71335-1131-47133511310415 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-4)Marketed from Mar 5, 2019
71335-1131-571335113105180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-5)Marketed from Mar 5, 2019
71335-1131-67133511310628 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-6)Marketed from Mar 5, 2019
71335-1131-77133511310710 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1131-7)Marketed from Mar 5, 2019

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
Generic name (nonproprietary)
potassium chloride
Active ingredients
Potassium chloride — 750 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210733
Marketing start
Listing expires
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 71335-1131_33ddada2-1929-8271-e063-6394a90a49adSPL ID 33ddada2-1929-8271-e063-6394a90a49adSPL set ID ab147ac2-d7d5-46d1-a2de-d866219197c1RxCUI 628953UNII 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

N471335113101 followed by a unit qualifier and the quantity

Package 71335-1131-01. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Potassium Chloride Extended-release Tablets, USP 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 Extended-release Tablets, USP 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 210733

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

FDA NDC Directory listings under ANDA 210733
ProductStrengthForm · routeLabelerProduct NDC
Potassium ChloridePotassium chloride 750 mg/1Tablet, Extended releaseOralDirect_Rx72189-027
Potassium ChloridePotassium chloride 750 mg/1Tablet, Extended releaseOralStrides Pharma Science Limited64380-861
Potassium ChloridePotassium chloride 750 mg/1Tablet, Extended releaseOralNorthwind Health Company, LLC51655-706
Potassium ChloridePotassium chloride 600 mg/1Tablet, Extended releaseOralStrides Pharma Science Limited64380-860

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