NDC codes

FDA NDC Directory
Product NDC (as listed)50090-7236Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-7236Add 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
50090-7236-0500907236005009072360090 TABLET in 1 BOTTLE (50090-7236-0)Marketed from Aug 28, 2024

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)
Ezetimibe
Generic name (nonproprietary)
ezetimibe
Active ingredients
Ezetimibe — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
A-S Medication SolutionsNDC labeler code 50090
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209234
Marketing start
Listing expires
Other FDA classes
Decreased Cholesterol Absorption (Physiologic effect)
Identifiers
Product ID 50090-7236_6d15d418-3f41-4aca-aafb-a331a85df702SPL ID 6d15d418-3f41-4aca-aafb-a331a85df702SPL set ID dd8a09cb-f014-4650-9da2-4ad1581c9741RxCUI 349556UNII EOR26LQQ24
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

N450090723600 followed by a unit qualifier and the quantity

Package 50090-7236-00. 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 is 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 patients 10 …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50090-7236

What is NDC 50090-7236?
50090-7236 is the product NDC for Ezetimibe, Ezetimibe 10 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ezetimibe.
What is the active ingredient?
Ezetimibe.
Who is the labeler?
A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ezetimibe?
40 other product NDCs are listed under this name. See all Ezetimibe 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 Ezetimibe NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ezetimibeEzetimibe 10 mg/1TabletOralSafecor Health, LLC48433-16148433-0161-03
EzetimibeEzetimibe 10 mg/1TabletOralMacleods Pharmaceuticals Limited33342-37333342-0373-0733342-0373-1033342-0373-15
EzetimibeEzetimibe 10 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-78710135-0787-0510135-0787-3010135-0787-90
ezetimibeEzetimibe 10 mg/1TabletOralQuallent Pharmaceuticals Health LLC82009-02482009-0024-05
EzetimibeEzetimibe 10 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-62831722-0628-0131722-0628-0531722-0628-10+4 more
EzetimibeEzetimibe 10 mg/1TabletOralA-S Medication Solutions50090-768950090-7689-00
EzetimibeEzetimibe 10 mg/1TabletOralA-S Medication Solutions50090-769050090-7690-0050090-7690-01
EzetimibeEzetimibe 10 mg/1TabletOralBryant Ranch Prepack71335-309271335-3092-0171335-3092-0271335-3092-03+2 more
EzetimibeEzetimibe 10 mg/1TabletOralOrient Pharma Co., Ltd.76333-17076333-0170-1276333-0170-1376333-0170-14+1 more
EzetimibeEzetimibe 10 mg/1TabletOralA-S Medication Solutions50090-733850090-7338-00

All 41 Ezetimibe NDCs

Other NDCs under ANDA 209234

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

FDA NDC Directory listings under ANDA 209234
ProductStrengthForm · routeLabelerProduct NDC
EzetimibeEzetimibe 10 mg/1TabletOralMajor Pharmaceuticals0904-7103
EzetimibeEzetimibe 10 mg/1TabletOralA-S Medication Solutions50090-3657
EzetimibeEzetimibe 10 mg/1TabletOralAmerican Health Packaging60687-373
EzetimibeEzetimibe 10 mg/1TabletOralAscend Laboratories, LLC67877-490
EzetimibeEzetimibe 10 mg/1TabletOralProficient Rx LP71205-277
EzetimibeEzetimibe 10 mg/1TabletOralBryant Ranch Prepack71335-1127

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