Losartan Potassium And Hydrochlorothiazide NDC 72189-290

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-290Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0290Add 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
72189-290-90	72189029090	90 TABLET, FILM COATED in 1 BOTTLE (72189-290-90)Marketed from Nov 29, 2021

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 And Hydrochlorothiazide
Generic name (nonproprietary): losartan potassium and hydrochlorothiazide
Active ingredients: Losartan potassium — 100 mg/1Hydrochlorothiazide — 12.5 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: DirectRx
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202289
Marketing start: Nov 29, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers: Product ID 72189-290_2c294389-2485-bf83-e063-6394a90a70d2SPL ID 2c294389-2485-bf83-e063-6394a90a70d2SPL set ID d1ee193e-bf78-3134-e053-2a95a90a65d2RxCUI 979464UNII 3ST302B24A, 0J48LPH2TH
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

N472189029090 followed by a unit qualifier and the quantity

Package 72189-0290-90. 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 Jan 20, 2025.

Indications (excerpt from the label)

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 management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 202289

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

FDA NDC Directory listings under ANDA 202289
Product	Strength	Form · route	Labeler	Product NDC
Losartan potassium and Hydrochlorothiazide	Losartan potassium 100 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-2492
Losartan Potassium And Hydrochlorothiazide	Hydrochlorothiazide 25 mg/1; Losartan potassium 100 mg/1	Tablet, Film coatedOral	DirectRx	72189-289
Losartan Potassium And Hydrochlorothiazide	Hydrochlorothiazide 12.5 mg/1; Losartan potassium 50 mg/1	Tablet, Film coatedOral	DirectRx	72189-297
Losartan potassium and Hydrochlorothiazide	Losartan potassium 100 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-3048
Losartan potassium and Hydrochlorothiazide	Losartan potassium 50 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-050
Losartan potassium and Hydrochlorothiazide	Losartan potassium 100 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-051
Losartan potassium and Hydrochlorothiazide	Losartan potassium 100 mg/1; Hydrochlorothiazide 25 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-052