What is NDC 46708-446?

46708-446 is the product NDC for Losartan Potassium, Losartan potassium 50 mg/1 tablet, film coated, listed with the FDA by Alembic Pharmaceuticals Limited. It has 4 package NDCs, shown above in 10- and 11-digit form.

Alembic Pharmaceuticals Limited, NDC labeler code 46708. 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 46708-446 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)46708-446Labeler and product segments. Claims need a package NDC.

Product NDC at billing width46708-0446Add 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
46708-446-30	4670804463046708044630	30 TABLET, FILM COATED in 1 BOTTLE (46708-446-30)Marketed from May 23, 2016
46708-446-31	4670804463146708044631	100 TABLET, FILM COATED in 1 BOTTLE (46708-446-31)Marketed from May 23, 2016
46708-446-90	4670804469046708044690	90 TABLET, FILM COATED in 1 BOTTLE (46708-446-90)Marketed from May 23, 2016
46708-446-91	4670804469146708044691	1000 TABLET, FILM COATED in 1 BOTTLE (46708-446-91)Marketed from May 23, 2016

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: Alembic Pharmaceuticals LimitedNDC labeler code 46708
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090428
Marketing start: May 23, 2016
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 46708-446_cedeb352-a540-4778-84e6-304f898fe17fSPL ID cedeb352-a540-4778-84e6-304f898fe17fSPL set ID eeb77c84-38d3-432d-914a-54b312b374bdRxCUI 979480, 979485, 979492UNII 3ST302B24AUPC 0346708447304, 0346708445300, 0346708446307
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

N446708044630 followed by a unit qualifier and the quantity

Package 46708-0446-30. 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

Current FDA label (SPL), effective Oct 8, 2025. 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 46708-446

What is NDC 46708-446?: 46708-446 is the product NDC for Losartan Potassium, Losartan potassium 50 mg/1 tablet, film coated, listed with the FDA by Alembic Pharmaceuticals Limited. It has 4 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?: Alembic Pharmaceuticals Limited, NDC labeler code 46708. 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 090428

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

FDA NDC Directory listings under ANDA 090428
Product	Strength	Form · route	Labeler	Product NDC
Losartan Potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-445
Losartan Potassium	Losartan potassium 100 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-447
Losartan Potassium	Losartan potassium 25 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-027
Losartan Potassium	Losartan potassium 50 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-028
Losartan Potassium	Losartan potassium 100 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-029