OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE NDC 72603-292

NDC codes

FDA NDC Directory

Product NDC (as listed)72603-292Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72603-0292Add 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
72603-292-01	72603029201	30 TABLET, FILM COATED in 1 BOTTLE (72603-292-01)Marketed from Apr 8, 2024
72603-292-02	72603029202	90 TABLET, FILM COATED in 1 BOTTLE (72603-292-02)Marketed from Apr 8, 2024

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): OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
Generic name (nonproprietary): olmesartan medoxomil and hydrochlorothiazide
Active ingredients: Olmesartan medoxomil — 40 mg/1Hydrochlorothiazide — 25 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: NorthStar RxLLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204801
Marketing start: Apr 8, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers: Product ID 72603-292_364af4fe-cde8-466f-b56f-d93d532b56f5SPL ID 364af4fe-cde8-466f-b56f-d93d532b56f5SPL set ID 364af4fe-cde8-466f-b56f-d93d532b56f5RxCUI 403853, 403854, 403855UNII 0J48LPH2TH, 6M97XTV3HDUPC 0372603292015, 0372603291018, 0372603291025, 0372603290011, 0372603292022
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

N472603029201 followed by a unit qualifier and the quantity

Package 72603-0292-01. 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 Apr 10, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Olmesartan medoxomil and hydrochlorothiazide tablets are indicated for the treatment of hypertension, to lower blood pressure. Olmesartan medoxomil and hydrochlorothiazide tablets are not indicated for the initial therapy of hypertension [see Dosage and Administration ( 2 )]. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including the class to which this drug principally belongs. There are no controlled trials demonstrating risk reduction with olmesartan medoxomil and hydrochlorothiazide…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 204801

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

FDA NDC Directory listings under ANDA 204801
Product	Strength	Form · route	Labeler	Product NDC
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	Olmesartan medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7571
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	Olmesartan medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-290
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	Olmesartan medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	NorthStar RxLLC	72603-291
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	Olmesartan medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4517
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	Olmesartan medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-175
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	Olmesartan medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-173
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	Olmesartan medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-174
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	Olmesartan medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7478
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	Olmesartan medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-3029
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	Olmesartan medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-3030
OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE	Olmesartan medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-3031