What is NDC 71085-083?

71085-083 is the product NDC for Potassium Chloride, Potassium chloride 3 g/3.16g for solution, listed with the FDA by IPG Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

IPG Pharmaceuticals, Inc., NDC labeler code 71085. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Potassium Chloride?

216 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Potassium Chloride NDC 71085-083 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71085-083Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71085-0083Add 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	Copy
71085-083-30	7108500833071085008330	30 POUCH in 1 CARTON (71085-083-30) / 3.16 g in 1 POUCH (71085-083-01)Marketed from Dec 1, 2025

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 — 3 g/3.16g
Dosage form: For solution
Route: Oral
Labeler: IPG Pharmaceuticals, Inc.NDC labeler code 71085
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 208019
Marketing start: Dec 1, 2025
Marketing end: Nov 30, 2028
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 71085-083_0f19da2c-a9ab-44fe-a38b-acb56c1c1883SPL ID 0f19da2c-a9ab-44fe-a38b-acb56c1c1883
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

N471085008330 followed by a unit qualifier and the quantity

Package 71085-0083-30. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 71085-083

What is NDC 71085-083?: 71085-083 is the product NDC for Potassium Chloride, Potassium chloride 3 g/3.16g for solution, listed with the FDA by IPG Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Potassium Chloride.
What is the active ingredient?: Potassium chloride.
Who is the labeler?: IPG Pharmaceuticals, Inc., NDC labeler code 71085. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Potassium Chloride?: 216 other product NDCs are listed under this name. See all Potassium Chloride NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Potassium Chloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Potassium Chloridepotassium chloride oral	Potassium chloride 1.5 g/15mL	SolutionOral	Cardinal Health 107, LLC	55154-8026	55154-8026-05
Potassium Chloride	Potassium chloride 1.5 g/1.58g	Powder, For solutionOral	Cardinal Health 107, LLC	55154-8352	55154-8352-05
Potassium Chloride	Potassium chloride 750 mg/1	Tablet, Film coated, Extended releaseOral	Coupler LLC	67046-1032	67046-1032-03
Potassium Chloride	Potassium chloride 750 mg/1	Tablet, Film coated, Extended releaseOral	St. Mary's Medical Park Pharmacy	60760-423	60760-0423-90
Potassium Chloride	Potassium chloride 750 mg/1	Tablet, Extended releaseOral	Northwind Health Company, LLC	82868-111	82868-0111-90
Potassium Chloride	Potassium chloride 20 meq/15mL	SolutionOral	Ajenat Pharmaceuticals LLC	82983-411	82983-0411-47
Potassium Chloride	Potassium chloride 40 meq/15mL	SolutionOral	Ajenat Pharmaceuticals LLC	82983-412	82983-0412-47
Potassium Chloride	Potassium chloride 20 meq/1	Tablet, Extended releaseOral	Major Pharmaceuticals	0904-7548	00904-7548-61
Potassium Chloride	Potassium chloride 20 meq/15mL	SolutionOral	Aurobindo Pharma Limited	59651-959	59651-0959-47
Potassium Chloride	Potassium chloride 40 meq/15mL	SolutionOral	Aurobindo Pharma Limited	59651-960	59651-0960-47

All 217 Potassium Chloride NDCs

Other NDCs under NDA 208019

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

FDA NDC Directory listings under NDA 208019
Product	Strength	Form · route	Labeler	Product NDC
Pokonzapotassium chloride	Potassium chloride .75 g/.79g	Powder, For solutionOral	Carwin Pharmaceutical Associates, LLC	15370-305
Pokonzapotassium chloride	Potassium chloride 1.125 g/1.185g	Powder, For solutionOral	Carwin Pharmaceutical Associates, LLC	15370-306
Potassium Chloride	Potassium chloride 1.5 g/1.58g	Powder, For solutionOral	Endo USA, Inc.	0603-1554
Potassium Chloride	Potassium chloride 1.5 g/1.58g	Powder, For solutionOral	Genus Lifesciences Inc.	64950-321