What is NDC 72162-2416?

72162-2416 is the product NDC for Nebivolol, Nebivolol hydrochloride 20 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Nebivolol?

89 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Nebivolol NDC 72162-2416 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72162-2416Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72162-2416Add 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	Copy
72162-2416-3	7216224160372162241603	30 TABLET in 1 BOTTLE (72162-2416-3)Marketed from Oct 31, 2024
72162-2416-9	7216224160972162241609	90 TABLET in 1 BOTTLE (72162-2416-9)Marketed from Oct 31, 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): Nebivolol
Generic name (nonproprietary): nebivolol
Active ingredients: Nebivolol hydrochloride — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 72162
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208717
Marketing start: Dec 29, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 72162-2416_02a4fc30-05ea-413a-89e5-a87a2bbf779bSPL ID 02a4fc30-05ea-413a-89e5-a87a2bbf779bSPL set ID 0ca84bf1-511d-480d-ba3d-0eef00ddad3eRxCUI 827073UNII JGS34J7L9I
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

N472162241603 followed by a unit qualifier and the quantity

Package 72162-2416-03. 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 Oct 31, 2024.

Indications (excerpt from the label)

Nebivolol is a beta-adrenergic blocking agent indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions.( 1.1 ) 1.1 Hypertension Nebivolol tablets are indicated for the treatment of hypertension, to lower blood pressure [ see Clinical Studies ( 14.1 ) ]. Nebivolol may be used alone or in combination with other antihypertensive agents [ see Drug Interactions ( 7 )]. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of ant…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2416

What is NDC 72162-2416?: 72162-2416 is the product NDC for Nebivolol, Nebivolol hydrochloride 20 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Nebivolol.
What is the active ingredient?: Nebivolol hydrochloride.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nebivolol?: 89 other product NDCs are listed under this name. See all Nebivolol 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 Nebivolol NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Nebivolol	Nebivolol 20 mg/1	TabletOral	Major Pharmaceuticals	0904-7500	00904-7500-04
Nebivolol	Nebivolol hydrochloride 5 mg/1	TabletOral	REMEDYREPACK INC.	70518-4648	70518-4648-00
Nebivolol	Nebivolol hydrochloride 2.5 mg/1	TabletOral	NorthStar RxLLC	72603-870	72603-0870-01
Nebivolol	Nebivolol hydrochloride 5 mg/1	TabletOral	NorthStar RxLLC	72603-871	72603-0871-0172603-0871-02
Nebivolol	Nebivolol hydrochloride 10 mg/1	TabletOral	NorthStar RxLLC	72603-872	72603-0872-0172603-0872-02
Nebivolol	Nebivolol hydrochloride 20 mg/1	TabletOral	NorthStar RxLLC	72603-873	72603-0873-0172603-0873-02
Nebivolol	Nebivolol 2.5 mg/1	TabletOral	Major Pharmaceuticals	0904-7497	00904-7497-04
Nebivolol	Nebivolol 5 mg/1	TabletOral	Major Pharmaceuticals	0904-7498	00904-7498-04
Nebivolol	Nebivolol 10 mg/1	TabletOral	Major Pharmaceuticals	0904-7499	00904-7499-04
Nebivolol	Nebivolol hydrochloride 2.5 mg/1	TabletOral	Macleods Pharmaceuticals Limited	33342-457	33342-0457-0733342-0457-1033342-0457-25

All 90 Nebivolol NDCs

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
Product	Strength	Form · route	Labeler	Product NDC
Nebivolol	Nebivolol hydrochloride 2.5 mg/1	TabletOral	Cadila Pharmaceuticals Limited	71209-058
Nebivolol	Nebivolol hydrochloride 5 mg/1	TabletOral	Cadila Pharmaceuticals Limited	71209-059
Nebivolol	Nebivolol hydrochloride 10 mg/1	TabletOral	Cadila Pharmaceuticals Limited	71209-060
Nebivolol	Nebivolol hydrochloride 20 mg/1	TabletOral	Cadila Pharmaceuticals Limited	71209-061
Nebivolol	Nebivolol hydrochloride 10 mg/1	TabletOral	Bryant Ranch Prepack	72162-2414
Nebivolol	Nebivolol hydrochloride 2.5 mg/1	TabletOral	Bryant Ranch Prepack	72162-2415
Nebivolol	Nebivolol hydrochloride 5 mg/1	TabletOral	Bryant Ranch Prepack	72162-2417
Nebivolol	Nebivolol hydrochloride 2.5 mg/1	TabletOral	Modavar Pharmaceuticals LLC	72241-032
Nebivolol	Nebivolol hydrochloride 5 mg/1	TabletOral	Modavar Pharmaceuticals LLC	72241-033
Nebivolol	Nebivolol hydrochloride 10 mg/1	TabletOral	Modavar Pharmaceuticals LLC	72241-034
Nebivolol	Nebivolol hydrochloride 20 mg/1	TabletOral	Modavar Pharmaceuticals LLC	72241-035