NDC codes

FDA NDC Directory
Product NDC (as listed)72241-034Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72241-0034Add 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
72241-034-047224100340490 TABLET in 1 BOTTLE (72241-034-04)Marketed from Dec 18, 2021
72241-034-0572241003405100 TABLET in 1 BOTTLE (72241-034-05)Marketed from Dec 18, 2021
72241-034-11722410034111000 TABLET in 1 BOTTLE (72241-034-11)Marketed from Dec 18, 2021
72241-034-227224100342230 TABLET in 1 BOTTLE (72241-034-22)Marketed from Dec 18, 2021

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)
Nebivolol
Generic name (nonproprietary)
nebivolol
Active ingredients
Nebivolol hydrochloride — 10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208717
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 72241-034_53d2f49b-b0b8-46fc-b80d-1ac3756e7e7cSPL ID 53d2f49b-b0b8-46fc-b80d-1ac3756e7e7cSPL set ID 19d20396-ade8-400e-94f4-69913637d051RxCUI 387013, 751612, 751618, 827073UNII JGS34J7L9IUPC 0372241032110, 0372241034053, 0372241034220, 0372241033223, 0372241035227, 0372241033117
Pharmacologic class
beta-Adrenergic 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

N472241003404 followed by a unit qualifier and the quantity

Package 72241-0034-04. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 208717

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

FDA NDC Directory listings under ANDA 208717
ProductStrengthForm · routeLabelerProduct NDC
NebivololNebivolol hydrochloride 2.5 mg/1TabletOralBryant Ranch Prepack72162-2415
NebivololNebivolol hydrochloride 10 mg/1TabletOralBryant Ranch Prepack72162-2414
NebivololNebivolol hydrochloride 20 mg/1TabletOralBryant Ranch Prepack72162-2416
NebivololNebivolol hydrochloride 5 mg/1TabletOralBryant Ranch Prepack72162-2417
NebivololNebivolol hydrochloride 10 mg/1TabletOralCadila Pharmaceuticals Limited71209-060
NebivololNebivolol hydrochloride 2.5 mg/1TabletOralModavar Pharmaceuticals LLC72241-032
NebivololNebivolol hydrochloride 2.5 mg/1TabletOralCadila Pharmaceuticals Limited71209-058
NebivololNebivolol hydrochloride 5 mg/1TabletOralModavar Pharmaceuticals LLC72241-033
NebivololNebivolol hydrochloride 5 mg/1TabletOralCadila Pharmaceuticals Limited71209-059
NebivololNebivolol hydrochloride 20 mg/1TabletOralModavar Pharmaceuticals LLC72241-035
NebivololNebivolol hydrochloride 20 mg/1TabletOralCadila Pharmaceuticals Limited71209-061

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