What is NDC 50090-5480?

50090-5480 is the product NDC for Losartan Potassium, Losartan potassium 50 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 3 package NDCs, shown above in 10- and 11-digit form.

A-S Medication Solutions, NDC labeler code 50090. 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 50090-5480 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-5480Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-5480Add 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
50090-5480-0	5009054800050090548000	30 TABLET in 1 BOTTLE (50090-5480-0)Marketed from Mar 8, 2021
50090-5480-1	5009054800150090548001	90 TABLET in 1 BOTTLE (50090-5480-1)Marketed from Sep 20, 2021
50090-5480-2	5009054800250090548002	100 TABLET in 1 BOTTLE (50090-5480-2)Marketed from Mar 9, 2023

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: A-S Medication SolutionsNDC labeler code 50090
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078232
Marketing start: Nov 1, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 50090-5480_e956cb01-a44e-4855-9359-ce5787862311SPL ID e956cb01-a44e-4855-9359-ce5787862311SPL set ID 0e0a06f3-b8bd-4178-a519-ed80362e33c2RxCUI 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

N450090548000 followed by a unit qualifier and the quantity

Package 50090-5480-00. 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 Mar 12, 2023. This label includes a boxed warning.

Indications (excerpt from the label)

Losartan potassium tablet USP is an 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 table…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50090-5480

What is NDC 50090-5480?: 50090-5480 is the product NDC for Losartan Potassium, Losartan potassium 50 mg/1 tablet, listed with the FDA by A-S Medication Solutions. 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?: A-S Medication Solutions, NDC labeler code 50090. 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 078232

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

FDA NDC Directory listings under ANDA 078232
Product	Strength	Form · route	Labeler	Product NDC
Losartan Potassium	Losartan potassium 100 mg/1	TabletOral	A-S Medication Solutions	50090-3403
Losartan Potassium	Losartan potassium 25 mg/1	TabletOral	A-S Medication Solutions	50090-5626
Losartan Potassium	Losartan potassium 25 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-210
Losartan Potassium	Losartan potassium 50 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-211
Losartan Potassium	Losartan potassium 100 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-212
Losartan Potassium	Losartan potassium 25 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-307
Losartan Potassium	Losartan potassium 50 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-308
Losartan Potassium	Losartan potassium 100 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-309
Losartan Potassium	Losartan potassium 25 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-376
Losartan Potassium	Losartan potassium 50 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-377
Losartan Potassium	Losartan potassium 100 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-378
Losartan Potassium	Losartan potassium 50 mg/1	TabletOral	REMEDYREPACK INC.	70518-3282