NDC codes

FDA NDC Directory
Product NDC (as listed)68462-226Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68462-0226Add 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
68462-226-0568462022605500 TABLET in 1 BOTTLE (68462-226-05)Marketed from Apr 29, 2022
68462-226-10684620226101000 TABLET in 1 BOTTLE (68462-226-10)Marketed from Apr 29, 2022
68462-226-116846202261110 BLISTER PACK in 1 CARTON (68462-226-11) / 10 TABLET in 1 BLISTER PACKMarketed from Apr 29, 2022
68462-226-306846202263030 TABLET in 1 BOTTLE (68462-226-30)Marketed from Apr 29, 2022
68462-226-906846202269090 TABLET in 1 BOTTLE (68462-226-90)Marketed from Apr 29, 2022

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)
Ezetimibe
Generic name (nonproprietary)
ezetimibe
Active ingredients
Ezetimibe — 10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078560
Marketing start
Marketing end
Other FDA classes
Decreased Cholesterol Absorption (Physiologic effect)
Identifiers
Product ID 68462-226_5009c162-91bb-425a-a688-6237c259d33eSPL ID 5009c162-91bb-425a-a688-6237c259d33eSPL set ID ac539a72-77e4-419c-b1d9-42002e9cecf7RxCUI 349556UNII EOR26LQQ24UPC 0368462226308
Pharmacologic class
Dietary Cholesterol Absorption Inhibitor

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

N468462022605 followed by a unit qualifier and the quantity

Package 68462-0226-05. 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 .

Indications (excerpt from the label)

Ezetimibe tablets are indicated: • In combination with a statin, or alone when additional low-density lipoprotein cholesterol (LDL-C) lowering therapy is not possible, as an adjunct to diet to reduce elevated LDL-C in adults with primary hyperlipidemia, including heterozygous familial hypercholesterolemia (HeFH). • In combination with a statin as an adjunct to diet to reduce elevated LDL-C in pediatric patients 10 years of age and older with HeFH. • In combination with fenofibrate as an adjunct to diet to reduce elevated LDL-C in adults with mixed hyperlipidemia. • In combination with a statin, and other LDL-C lowering therapies, to reduce elevated LDL-C levels in adults and in pediatric pat…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 078560

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

FDA NDC Directory listings under ANDA 078560
ProductStrengthForm · routeLabelerProduct NDC
EzetimibeEzetimibe 10 mg/1TabletOralA-S Medication Solutions50090-7338
EzetimibeEzetimibe 10 mg/1TabletOralA-S Medication Solutions50090-7339
EzetimibeEzetimibe 10 mg/1TabletOralProficient Rx LP82804-211

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