What is NDC 72162-2507?

72162-2507 is the product NDC for Losartan Potassium, Losartan potassium 50 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 3 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 72162. 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 72162-2507 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72162-2507Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72162-2507Add 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
72162-2507-0	7216225070072162250700	1000 TABLET in 1 BOTTLE (72162-2507-0)Marketed from May 19, 2025
72162-2507-3	7216225070372162250703	30 TABLET in 1 BOTTLE (72162-2507-3)Marketed from May 19, 2025
72162-2507-9	7216225070972162250709	90 TABLET in 1 BOTTLE (72162-2507-9)Marketed from May 19, 2025

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
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 72162
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203030
Marketing start: Oct 14, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 72162-2507_3585dbef-6405-e0ff-e063-6394a90a3833SPL ID 3585dbef-6405-e0ff-e063-6394a90a3833SPL set ID 3585b1d3-ccb7-747e-e063-6294a90a4b77RxCUI 979492UNII 3ST302B24A
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

N472162250700 followed by a unit qualifier and the quantity

Package 72162-2507-00. 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 May 19, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Losartan potassium tablets are angiotensin II receptor blocker (ARB) indicated for: Treatment of hypertension, to lower blood pressure in adults and children greater than 6 years old. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) Reduction of the risk of stroke in patients with hypertension and left ventricular hypertrophy. There is evidence that this benefit does not apply to Black patients. ( 1.2 ) Treatment of diabetic nephropathy with an elevated serum creatinine and proteinuria in patients with type 2 diabetes and a history of hypertension. ( 1.3 ) 1.1 Hypertension Losartan potassium tablets ar…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2507

What is NDC 72162-2507?: 72162-2507 is the product NDC for Losartan Potassium, Losartan potassium 50 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 3 package NDCs, 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?: Bryant Ranch Prepack, NDC labeler code 72162. 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 203030

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

FDA NDC Directory listings under ANDA 203030
Product	Strength	Form · route	Labeler	Product NDC
Losartan Potassium	Losartan potassium 25 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-144
Losartan Potassium	Losartan potassium 50 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-145
Losartan Potassium	Losartan potassium 100 mg/1	TabletOral	Unichem Pharmaceuticals (USA), Inc.	29300-146
Losartan Potassium	Losartan potassium 25 mg/1	TabletOral	Bryant Ranch Prepack	72162-2506
Losartan Potassium	Losartan potassium 100 mg/1	TabletOral	Bryant Ranch Prepack	72162-2508