Ezetimibe NDC 71335-3092

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-3092Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-3092Add 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 NDC	11-digit (billing)	Package
71335-3092-1	71335309201	30 TABLET in 1 BOTTLE (71335-3092-1)Marketed from Feb 17, 2026
71335-3092-2	71335309202	90 TABLET in 1 BOTTLE (71335-3092-2)Marketed from Feb 17, 2026
71335-3092-3	71335309203	28 TABLET in 1 BOTTLE (71335-3092-3)Marketed from Feb 17, 2026
71335-3092-4	71335309204	18 TABLET in 1 BOTTLE (71335-3092-4)Marketed from Feb 17, 2026
71335-3092-5	71335309205	60 TABLET in 1 BOTTLE (71335-3092-5)Marketed from Feb 17, 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): Ezetimibe
Generic name (nonproprietary): ezetimibe
Active ingredients: Ezetimibe — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch Prepack
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210859
Marketing start: Jul 26, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Decreased Cholesterol Absorption (Physiologic effect)
Identifiers: Product ID 71335-3092_1329fd6e-ab21-40be-8584-6886362ab4b6SPL ID 1329fd6e-ab21-40be-8584-6886362ab4b6SPL set ID 02b00cb2-7253-4fb4-a216-53691a929a28RxCUI 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

N471335309201 followed by a unit qualifier and the quantity

Package 71335-3092-01. 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

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