What is NDC 60760-876?

60760-876 is the product NDC for Losartan potassium, Losartan potassium 50 mg/1 tablet, film coated, listed with the FDA by St. Mary's Medical Park Pharmacy. It has 1 package NDC, shown above in 10- and 11-digit form.

St. Mary's Medical Park Pharmacy, NDC labeler code 60760. 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 60760-876 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)60760-876Labeler and product segments. Claims need a package NDC.

Product NDC at billing width60760-0876Add 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
60760-876-30	6076008763060760087630	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-876-30)Marketed from Nov 2, 2026

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): Losartan potassium
Generic name (nonproprietary): losartan potassium
Active ingredients: Losartan potassium — 50 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: St. Mary's Medical Park PharmacyNDC labeler code 60760
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217396
Marketing start: Nov 2, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 60760-876_5f67878c-be27-db50-e063-6294a90ac95aSPL ID 5f67878c-be27-db50-e063-6294a90ac95a
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

N460760087630 followed by a unit qualifier and the quantity

Package 60760-0876-30. 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 60760-876

What is NDC 60760-876?: 60760-876 is the product NDC for Losartan potassium, Losartan potassium 50 mg/1 tablet, film coated, listed with the FDA by St. Mary's Medical Park Pharmacy. 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?: St. Mary's Medical Park Pharmacy, NDC labeler code 60760. 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 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
Losartan Potassium	Losartan potassium 50 mg/1	TabletOral	AiPing Pharmaceutical, Inc.	11788-101	11788-0101-1011788-0101-3011788-0101-90

All 174 Losartan potassium NDCs

Other NDCs under ANDA 217396

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

FDA NDC Directory listings under ANDA 217396
Product	Strength	Form · route	Labeler	Product NDC
Losartan potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-1470
Losartan potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4091
Losartan potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Novadoz Pharmaceuticals LLC	72205-141
Losartan potassium	Losartan potassium 50 mg/1	Tablet, Film coatedOral	Novadoz Pharmaceuticals LLC	72205-142
Losartan potassium	Losartan potassium 100 mg/1	Tablet, Film coatedOral	Novadoz Pharmaceuticals LLC	72205-143