What is NDC 68071-1517?

68071-1517 is the product NDC for Losartan Potassium, Losartan potassium 50 mg/1 tablet, film coated, listed with the FDA by NuCare Pharmaceuticals,iNc.. It has 1 package NDC, shown above in 10- and 11-digit form.

NuCare Pharmaceuticals,iNc., NDC labeler code 68071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Losartan Potassium?

173 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Losartan Potassium NDC 68071-1517 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68071-1517Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68071-1517Add 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
68071-1517-9	6807115170968071151709	90 TABLET, FILM COATED in 1 BOTTLE (68071-1517-9)Marketed from Jul 19, 2017

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): Losartan Potassium
Generic name (nonproprietary): losartan potassium
Active ingredients: Losartan potassium — 50 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: NuCare Pharmaceuticals,iNc.NDC labeler code 68071
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 091497
Marketing start: Jul 30, 2014
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 68071-1517_1d79a464-4b98-b1e6-e063-6394a90aab58SPL ID 1d79a464-4b98-b1e6-e063-6394a90aab58SPL set ID 54b363c4-00bb-08db-e054-00144ff8d46cRxCUI 979492UNII 3ST302B24AUPC 0368071151794
Pharmacologic class: Angiotensin 2 Receptor Blocker

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

N468071151709 followed by a unit qualifier and the quantity

Package 68071-1517-09. 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 Jul 17, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hypertension Losartan potassium tablets USP are indicated for the treatment of hypertension. It may be used alone or in combination with other antihypertensive agents, including diuretics. Hypertensive Patients with Left Ventricular Hypertrophy Losartan potassium tablets USP are indicated to reduce the risk of stroke in patients with hypertension and left ventricular hypertrophy, but there is evidence that this benefit does not apply to Black patients. (See PRECAUTIONS, Race and CLINICAL PHARMACOLOGY, Pharmacodynamics and Clinical Effects, Reduction in the Risk of Stroke, Race.) Nephropathy in Type 2 Diabetic Patients Losartan potassium tablets USP are indicated for the…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68071-1517

What is NDC 68071-1517?: 68071-1517 is the product NDC for Losartan Potassium, Losartan potassium 50 mg/1 tablet, film coated, listed with the FDA by NuCare Pharmaceuticals,iNc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Losartan Potassium.
What is the active ingredient?: Losartan potassium.
Who is the labeler?: NuCare Pharmaceuticals,iNc., NDC labeler code 68071. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Losartan Potassium?: 173 other product NDCs are listed under this name. See all Losartan Potassium 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 Losartan Potassium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Losartan potassium	Losartan potassium 50 mg/1	Tablet, Film coatedOral	St. Mary's Medical Park Pharmacy	60760-876	60760-0876-30
Losartan potassium	Losartan potassium 100 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4773	70518-4773-00
Losartan Potassiumlosartan	Losartan potassium 50 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4160	68788-4160-0368788-4160-09
Losartan Potassium	Losartan potassium 100 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4695	70518-4695-0070518-4695-01
Losartan Potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Unit Dose Solutions, Inc.	87441-052	87441-0052-01
Losartan Potassium	Losartan potassium 50 mg/1	Tablet, Film coatedOral	Unit Dose Solutions, Inc.	87441-053	87441-0053-01
Losartan Potassium	Losartan potassium 100 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0702	67046-0702-03
Losartan potassium	Losartan potassium 50 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4127	68788-4127-0368788-4127-09
Losartan Potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1088	67046-1088-03
Losartan potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4091	68788-4091-0368788-4091-09

All 174 Losartan Potassium NDCs

Other NDCs under ANDA 091497

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

FDA NDC Directory listings under ANDA 091497
Product	Strength	Form · route	Labeler	Product NDC
Losartan Potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Solco Healthcare US, LLC	43547-360
Losartan Potassium	Losartan potassium 50 mg/1	Tablet, Film coatedOral	Solco Healthcare US, LLC	43547-361
Losartan Potassium	Losartan potassium 100 mg/1	Tablet, Film coatedOral	Solco Healthcare US, LLC	43547-362
Losartan Potassium	Losartan potassium 100 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-808
Losartan Potassium	Losartan potassium 50 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-830
Losartan Potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1088
Losartan Potassium	Losartan potassium 50 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals,Inc.	68071-2690
Losartan Potassium	Losartan potassium 100 mg/1	Tablet, Film coatedOral	NuCare Pharmaceuticals.Inc.	68071-3846
Losartan Potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4007
Losartan Potassium	Losartan potassium 100 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8186
Losartan Potassium	Losartan potassium 50 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8189
Losartan Potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-3489
Losartan Potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-226
Losartan Potassium	Losartan potassium 50 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-0262
Losartan Potassium	Losartan potassium 100 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2083
Losartan Potassium	Losartan potassium 50 mg/1	Tablet, Film coatedOral	Aphena Pharma Solutions - Tennessee, LLC	71610-207
Losartan Potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Aphena Pharma Solutions - Tennessee, LLC	71610-224
Losartan Potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	DIRECT RX	72189-100
Losartan Potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Unit Dose Solutions, Inc.	87441-052