NDC codes

FDA NDC Directory
Product NDC (as listed)73190-078Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73190-0078Add 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
73190-078-90731900078907319000789090 TABLET, FILM COATED in 1 BOTTLE (73190-078-90)Marketed from Jul 14, 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

Generic name (nonproprietary)
olmesartan medoxomil-hydrochlorothiazide
Active ingredients
Olmesartan medoxomil — 20 mg/1Hydrochlorothiazide — 12.5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
AvKARENDC labeler code 73190
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 021532
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 73190-078_569596ad-cf4a-80be-e063-6394a90aa2aaSPL ID 569596ad-cf4a-80be-e063-6394a90aa2aaSPL set ID 569596a2-98f0-116a-e063-6294a90a3fa1RxCUI 403853, 403854, 403855UNII 0J48LPH2TH, 6M97XTV3HD
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

N473190007890 followed by a unit qualifier and the quantity

Package 73190-0078-90. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

BENICAR HCT (olmesartan medoxomil and hydrochlorothiazide) is indicated for the treatment of hypertension, to lower blood pressure. BENICAR HCT is 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 BENICAR HCT. Control of high blood pressure should be part of comprehensive cardi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73190-078

What is NDC 73190-078?
73190-078 is the product NDC for olmesartan medoxomil-hydrochlorothiazide, Olmesartan medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 tablet, film coated, listed with the FDA by AvKARE. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
olmesartan medoxomil-hydrochlorothiazide.
What is the active ingredient?
Olmesartan medoxomil, Hydrochlorothiazide.
Who is the labeler?
AvKARE, NDC labeler code 73190. 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-hydrochlorothiazide?
8 other product NDCs are listed under this name. See all olmesartan medoxomil-hydrochlorothiazide 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-hydrochlorothiazide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
olmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralAvKARE73190-07973190-0079-90
olmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1Tablet, Film coatedOralAvKARE73190-08073190-0080-90
olmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralNovadoz Pharmaceuticals LLC72205-14772205-0147-3072205-0147-9072205-0147-99
olmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralNovadoz Pharmaceuticals LLC72205-14872205-0148-3072205-0148-9072205-0148-99
olmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1Tablet, Film coatedOralNovadoz Pharmaceuticals LLC72205-14972205-0149-3072205-0149-9072205-0149-99
olmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralAvKARE42291-92442291-0924-90
olmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralAvKARE42291-92542291-0925-90
olmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1Tablet, Film coatedOralAvKARE42291-92642291-0926-90

Other NDCs under NDA 021532

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

FDA NDC Directory listings under NDA 021532
ProductStrengthForm · routeLabelerProduct NDC
Benicar HCTolmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralCosette Pharmaceuticals, Inc.0713-0863
Benicar HCTolmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralCosette Pharmaceuticals, Inc.0713-0864
Benicar HCTolmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1Tablet, Film coatedOralCosette Pharmaceuticals, Inc.0713-0865
Benicar HCTolmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralCosette Pharmaceuticals, Inc.0713-0943
Benicar HCTolmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralCosette Pharmaceuticals, Inc.0713-0944
Benicar HCTolmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1Tablet, Film coatedOralCosette Pharmaceuticals, Inc.0713-0945
olmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralAvKARE42291-924
olmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralAvKARE42291-925
olmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1Tablet, Film coatedOralAvKARE42291-926
olmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 12.5 mg/1Tablet, Film coatedOralAvKARE73190-079
olmesartan medoxomil-hydrochlorothiazideOlmesartan medoxomil 40 mg/1; Hydrochlorothiazide 25 mg/1Tablet, Film coatedOralAvKARE73190-080

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