What is NDC 72189-137?

72189-137 is the product NDC for Olmesartan Medoxomil, Olmesartan medoxomil 20 mg/1 tablet, film coated, listed with the FDA by direct rx. It has 2 package NDCs, shown above in 10- and 11-digit form.

direct rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Olmesartan Medoxomil?

122 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Olmesartan Medoxomil NDC 72189-137

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-137Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0137Add 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
72189-137-30	7218901373072189013730	30 TABLET, FILM COATED in 1 BOTTLE (72189-137-30)Marketed from Dec 2, 2020
72189-137-90	7218901379072189013790	90 TABLET, FILM COATED in 1 BOTTLE (72189-137-90)Marketed from Dec 2, 2020

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 medoxomil — 20 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: direct rxNDC labeler code 72189
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207662
Marketing start: Dec 2, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers: Product ID 72189-137_2becff06-7cc1-1200-e063-6294a90ad1ecSPL ID 2becff06-7cc1-1200-e063-6294a90ad1ecSPL set ID b57e47a5-43e0-d1c5-e053-2a95a90a2b07RxCUI 349401, 349405UNII 6M97XTV3HD
Pharmacologic class: Angiotensin 2 Receptor Blocker

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

N472189013730 followed by a unit qualifier and the quantity

Package 72189-0137-30. 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 Jan 17, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Olmesartan medoxomil tablets are indicated for the treatment of hypertension, 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. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessat…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-137

What is NDC 72189-137?: 72189-137 is the product NDC for Olmesartan Medoxomil, Olmesartan medoxomil 20 mg/1 tablet, film coated, listed with the FDA by direct rx. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Olmesartan Medoxomil.
What is the active ingredient?: Olmesartan medoxomil.
Who is the labeler?: direct rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Olmesartan Medoxomil?: 122 other product NDCs are listed under this name. See all Olmesartan Medoxomil NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Olmesartan Medoxomil NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Olmesartan medoxomil	Olmesartan medoxomil 5 mg/1	TabletOral	NorthStar RxLLC	72603-950	72603-0950-0172603-0950-02
Olmesartan medoxomil	Olmesartan medoxomil 20 mg/1	TabletOral	NorthStar RxLLC	72603-951	72603-0951-0172603-0951-02
Olmesartan medoxomil	Olmesartan medoxomil 40 mg/1	TabletOral	NorthStar RxLLC	72603-952	72603-0952-0172603-0952-02
Olmesartan Medoxomil	Olmesartan medoxomil 5 mg/1	Tablet, Film coatedOral	HEC Pharm USA Inc.	72303-0848	72303-0848-0172303-0848-02
Olmesartan Medoxomil	Olmesartan medoxomil 20 mg/1	Tablet, Film coatedOral	HEC Pharm USA Inc.	72303-0849	72303-0849-0172303-0849-02
Olmesartan Medoxomil	Olmesartan medoxomil 40 mg/1	Tablet, Film coatedOral	HEC Pharm USA Inc.	72303-0850	72303-0850-0172303-0850-02
Olmesartan medoxomil	Olmesartan medoxomil 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4598	70518-4598-00
Olmesartan Medoxomil	Olmesartan medoxomil 40 mg/1	TabletOral	Umedica Laboratories USA Inc.	60290-011	60290-0011-0160290-0011-0260290-0011-03
Olmesartan Medoxomil	Olmesartan medoxomil 5 mg/1	TabletOral	Umedica Laboratories USA Inc.	60290-009	60290-0009-0160290-0009-0260290-0009-03
Olmesartan Medoxomil	Olmesartan medoxomil 20 mg/1	TabletOral	Umedica Laboratories USA Inc.	60290-010	60290-0010-0160290-0010-0260290-0010-03

All 123 Olmesartan Medoxomil NDCs

Other NDCs under ANDA 207662

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

FDA NDC Directory listings under ANDA 207662
Product	Strength	Form · route	Labeler	Product NDC
olmesartan medoxomil	Olmesartan medoxomil 5 mg/1	Tablet, Film coatedOral	Accord Healthcare Inc.	16729-320
olmesartan medoxomil	Olmesartan medoxomil 20 mg/1	Tablet, Film coatedOral	Accord Healthcare Inc.	16729-321
olmesartan medoxomil	Olmesartan medoxomil 40 mg/1	Tablet, Film coatedOral	Accord Healthcare Inc.	16729-322
olmesartan medoxomil	Olmesartan medoxomil 20 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-3471
olmesartan medoxomil	Olmesartan medoxomil 40 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-3487
olmesartan medoxomil	Olmesartan medoxomil 20 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-6606
olmesartan medoxomil	Olmesartan medoxomil 5 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-9426
olmesartan medoxomil	Olmesartan medoxomil 20 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-0775
olmesartan medoxomil	Olmesartan medoxomil 40 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-0817
Olmesartan Medoxomil	Olmesartan medoxomil 40 mg/1	Tablet, Film coatedOral	direct rx	72189-138
Olmesartan Medoxomil	Olmesartan medoxomil 5 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-373