NDC codes

FDA NDC Directory
Product NDC (as listed)65862-857Labeler and product segments. Claims need a package NDC.
Product NDC at billing width65862-0857Add 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
65862-857-306586208573030 TABLET, FILM COATED in 1 BOTTLE (65862-857-30)Marketed from May 15, 2017

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)
Amlodipine and Olmesartan Medoxomil
Generic name (nonproprietary)
amlodipine and olmesartan medoxomil
Active ingredients
Amlodipine besylate10 mg/1Olmesartan medoxomil40 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206906
Marketing start
Listing expires
Other FDA classes
Angiotensin 2 Receptor Antagonists (Mechanism)Calcium Channel Antagonists (Mechanism)Cytochrome P450 3A Inhibitors (Mechanism)Dihydropyridines (Chemical structure)
Identifiers
Product ID 65862-857_4879a01c-0ba7-4d27-9847-f22e8546fa8fSPL ID 4879a01c-0ba7-4d27-9847-f22e8546fa8fSPL set ID b13a8b46-104e-4b75-8f4a-928d2204eff5RxCUI 730861, 730866, 730869, 730872UNII 864V2Q084H, 6M97XTV3HDUPC 0365862855305, 0365862856302, 0365862854308, 0365862857309
Pharmacologic class
Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel 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

N465862085730 followed by a unit qualifier and the quantity

Package 65862-0857-30. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Amlodipine and olmesartan medoxomil tablets are indicated for the treatment of hypertension, alone or with other antihypertensive agents, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular (CV) 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 amlodipine and olmesartan medoxomil tablets. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 206906

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

FDA NDC Directory listings under ANDA 206906
ProductStrengthForm · routeLabelerProduct NDC
Amlodipine and Olmesartan MedoxomilAmlodipine besylate 10 mg/1; Olmesartan medoxomil 20 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-856
Amlodipine and Olmesartan MedoxomilAmlodipine besylate 5 mg/1; Olmesartan medoxomil 20 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-854
Amlodipine and Olmesartan MedoxomilAmlodipine besylate 5 mg/1; Olmesartan medoxomil 40 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-855
Amlodipine and Olmesartan MedoxomilAmlodipine besylate 5 mg/1; Olmesartan medoxomil 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-7863

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