NDC codes

FDA NDC Directory
Product NDC (as listed)72603-951Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72603-0951Add 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
72603-951-017260309510130 TABLET in 1 BOTTLE (72603-951-01)Marketed from Aug 7, 2026
72603-951-027260309510290 TABLET in 1 BOTTLE (72603-951-02)Marketed from Aug 7, 2026

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
Generic name (nonproprietary)
olmesartan medoxomil
Active ingredients
Olmesartan medoxomil20 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204814
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 72603-951_812d2d57-14d6-48a9-9687-85c2d125197eSPL ID 812d2d57-14d6-48a9-9687-85c2d125197eSPL set ID 812d2d57-14d6-48a9-9687-85c2d125197eRxCUI 349373, 349401, 349405UNII 6M97XTV3HDUPC 0372603952025

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

N472603095101 followed by a unit qualifier and the quantity

Package 72603-0951-01. 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)

Olmesartan medoxomil tablets are indicated for the treatment of hypertension in adults and children six years of age and older, to lower blood pressure. 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 tablets. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, d

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 204814

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

FDA NDC Directory listings under ANDA 204814
ProductStrengthForm · routeLabelerProduct NDC
Olmesartan medoxomilOlmesartan medoxomil 5 mg/1TabletOralNorthStar RxLLC72603-950
Olmesartan medoxomilOlmesartan medoxomil 40 mg/1TabletOralNorthStar RxLLC72603-952
Olmesartan medoxomilOlmesartan medoxomil 5 mg/1TabletOralMacleods Pharmaceuticals Limited33342-178
Olmesartan medoxomilOlmesartan medoxomil 20 mg/1TabletOralMacleods Pharmaceuticals Limited33342-179
Olmesartan medoxomilOlmesartan medoxomil 40 mg/1TabletOralMacleods Pharmaceuticals Limited33342-180
Olmesartan medoxomilOlmesartan medoxomil 20 mg/1TabletOralREMEDYREPACK INC.70518-4598
Olmesartan medoxomilOlmesartan medoxomil 40 mg/1TabletOralA-S Medication Solutions50090-6632
Olmesartan medoxomilOlmesartan medoxomil 40 mg/1TabletOralA-S Medication Solutions50090-6633

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