NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2996Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2996Add 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
71335-2996-17133529960190 TABLET, COATED in 1 BOTTLE (71335-2996-1)Marketed from Feb 4, 2026
71335-2996-27133529960230 TABLET, COATED in 1 BOTTLE (71335-2996-2)Marketed from Feb 4, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 5 mg/1
Dosage form
Tablet, Coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208659
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)
Identifiers
Product ID 71335-2996_ad416720-0f92-4332-afcc-a65cd320781dSPL ID ad416720-0f92-4332-afcc-a65cd320781dSPL set ID 1df1ff60-6be5-4018-a28c-0d23e5867ebaRxCUI 349373UNII 6M97XTV3HD

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

N471335299601 followed by a unit qualifier and the quantity

Package 71335-2996-01. 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 tablet 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. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 208659

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

FDA NDC Directory listings under ANDA 208659
ProductStrengthForm · routeLabelerProduct NDC
Olmesartan MedoxomilOlmesartan medoxomil 5 mg/1Tablet, CoatedOralInventia Healthcare Limited49252-065
Olmesartan MedoxomilOlmesartan medoxomil 20 mg/1Tablet, CoatedOralInventia Healthcare Limited49252-066
Olmesartan MedoxomilOlmesartan medoxomil 40 mg/1Tablet, CoatedOralInventia Healthcare Limited49252-067
Olmesartan MedoxomilOlmesartan medoxomil 40 mg/1Tablet, CoatedOralRising Pharma Holdings, Inc.64980-603
Olmesartan MedoxomilOlmesartan medoxomil 20 mg/1Tablet, CoatedOralRising Pharma Holdings, Inc.64980-602
Olmesartan MedoxomilOlmesartan medoxomil 5 mg/1Tablet, CoatedOralRising Pharma Holdings, Inc.64980-665

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