NDC codes

FDA NDC Directory
Product NDC (as listed)62332-029Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62332-0029Add 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 NDC11-digit (billing)PackageCopy
62332-029-306233200293030 TABLET, FILM COATED in 1 BOTTLE (62332-029-30)Marketed from May 23, 2016
62332-029-3162332002931100 TABLET, FILM COATED in 1 BOTTLE (62332-029-31)Marketed from May 23, 2016
62332-029-906233200299090 TABLET, FILM COATED in 1 BOTTLE (62332-029-90)Marketed from May 23, 2016
62332-029-91623320029911000 TABLET, FILM COATED in 1 BOTTLE (62332-029-91)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 — 100 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090428
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 62332-029_a12a7eb0-196c-4ddc-ba64-2909f65b6f19SPL ID a12a7eb0-196c-4ddc-ba64-2909f65b6f19SPL set ID 1dadbe02-289c-4312-9e65-40f3314dcc31RxCUI 979480, 979485, 979492UNII 3ST302B24AUPC 0362332028306, 0362332027309, 0362332029303

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

N462332002930 followed by a unit qualifier and the quantity

Package 62332-0029-30. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Losartan potassium tablet 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 tab…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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
ProductStrengthForm · routeLabelerProduct NDC
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Inc.62332-027
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Inc.62332-028
Losartan PotassiumLosartan potassium 50 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-446
Losartan PotassiumLosartan potassium 25 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-445
Losartan PotassiumLosartan potassium 100 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-447

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