NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2662Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2662Add 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
71335-2662-17133526620130 TABLET, FILM COATED in 1 BOTTLE (71335-2662-1)Marketed from Jun 26, 2025
71335-2662-27133526620290 TABLET, FILM COATED in 1 BOTTLE (71335-2662-2)Marketed from Jun 26, 2025
71335-2662-371335266203120 TABLET, FILM COATED in 1 BOTTLE (71335-2662-3)Marketed from Jun 26, 2025
71335-2662-471335266204100 TABLET, FILM COATED in 1 BOTTLE (71335-2662-4)Marketed from Jun 26, 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 and hydrochlorothiazide
Generic name (nonproprietary)
losartan potassium and hydrochlorothiazide
Active ingredients
Hydrochlorothiazide — 12.5 mg/1Losartan 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 204832
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 71335-2662_de121cef-3137-4100-9489-f7c6a50faba8SPL ID de121cef-3137-4100-9489-f7c6a50faba8SPL set ID eb423f4b-8104-4406-bfc2-8943e517329fRxCUI 979464UNII 0J48LPH2TH, 3ST302B24A
Pharmacologic class
Angiotensin 2 Receptor Blocker; Thiazide Diuretic

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

N471335266201 followed by a unit qualifier and the quantity

Package 71335-2662-01. 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 and hydrochlorothiazide tablets are combination of losartan, an angiotensin II receptor blocker (ARB) and hydrochlorothiazide, a diuretic indicated for: 1.1 Hypertension Losartan potassium and hydrochlorothiazide tablets are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular (CV) events, primarily strokes and myocardial infarction. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including losartan and hydrochlorothiazide. Control of high blood pressure should be part of comprehensive cardiovascular risk m…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 204832

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

FDA NDC Directory listings under ANDA 204832
ProductStrengthForm · routeLabelerProduct NDC
losartan potassium and hydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Losartan potassium 50 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2462
losartan potassium and hydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Losartan potassium 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2461
losartan potassium and hydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Losartan potassium 50 mg/1Tablet, Film coatedOralUnichem Pharmaceuticals (USA), Inc.29300-190
losartan potassium and hydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Losartan potassium 100 mg/1Tablet, Film coatedOralUnichem Pharmaceuticals (USA), Inc.29300-191
losartan potassium and hydrochlorothiazideHydrochlorothiazide 25 mg/1; Losartan potassium 100 mg/1Tablet, Film coatedOralUnichem Pharmaceuticals (USA), Inc.29300-192
losartan potassium and hydrochlorothiazideHydrochlorothiazide 25 mg/1; Losartan potassium 100 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-671
losartan potassium and hydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Losartan potassium 100 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2827

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