What is NDC 68180-799?

68180-799 is the product NDC for Potassium Chloride, Potassium chloride 10 meq/1 capsule, coated, extended release, listed with the FDA by Lupin Pharmaceuticals, Inc..

Lupin Pharmaceuticals, Inc., NDC labeler code 68180. 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?

217 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 68180-799 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68180-799Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68180-0799Add the package segment from the table below.

Product information

Brand name (proprietary): Potassium Chloride
Generic name (nonproprietary): potassium chloride
Active ingredients: Potassium chloride — 10 meq/1
Dosage form: Capsule, Coated, Extended release
Route: Oral
Labeler: Lupin Pharmaceuticals, Inc.NDC labeler code 68180
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203002
Marketing start: Jan 18, 2016
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 68180-799_d5646d4c-67ac-4e51-85a9-cc8a6e60bebeSPL ID d5646d4c-67ac-4e51-85a9-cc8a6e60bebeSPL set ID 1f33bcfe-c28a-4800-9241-685d974a5d91RxCUI 312504, 315183UNII 660YQ98I10UPC 0368180798019
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.

Product label

Current FDA label (SPL), effective Nov 8, 2023.

Indications (excerpt from the label)

Potassium chloride extended-release capsules are indicated for the treatment and prophylaxis of hypokalemia in adults and children 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 capsules, USP contain potassium chloride, 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)

About NDC 68180-799

What is NDC 68180-799?: 68180-799 is the product NDC for Potassium Chloride, Potassium chloride 10 meq/1 capsule, coated, extended release, listed with the FDA by Lupin Pharmaceuticals, Inc..
What drug is associated with this NDC?: Potassium Chloride.
What is the active ingredient?: Potassium chloride.
Who is the labeler?: Lupin Pharmaceuticals, Inc., NDC labeler code 68180. 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?: 217 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 3 g/3.16g	For solutionOral	IPG Pharmaceuticals, Inc.	71085-083	71085-0083-30
Potassium Chloride	Potassium chloride 20 meq/15mL	SolutionOral	Aurobindo Pharma Limited	59651-959	59651-0959-47

All 218 Potassium Chloride NDCs

Other NDCs under ANDA 203002

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

FDA NDC Directory listings under ANDA 203002
Product	Strength	Form · route	Labeler	Product NDC
Potassium Chloride	Potassium chloride 10 meq/1	Capsule, Coated, Extended releaseOral	A-S Medication Solutions	50090-4734