NDC codes

FDA NDC Directory
Product NDC (as listed)82804-120Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82804-0120Add 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
82804-120-90828040120908280401209090 TABLET in 1 BOTTLE (82804-120-90)Marketed from Jul 8, 2024

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 — 5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 82804
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203825
Marketing start
Listing expires
Other FDA classes
Adrenergic beta-Antagonists (Mechanism)
Identifiers
Product ID 82804-120_c6606db5-3937-4e90-9870-3cbfa4ec909eSPL ID c6606db5-3937-4e90-9870-3cbfa4ec909eSPL set ID c6606db5-3937-4e90-9870-3cbfa4ec909eRxCUI 387013UNII JGS34J7L9IUPC 0382804120901
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

N482804012090 followed by a unit qualifier and the quantity

Package 82804-0120-90. 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)

Nebivolol tablet 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 tablets 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 controlle…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82804-120

What is NDC 82804-120?
82804-120 is the product NDC for Nebivolol, Nebivolol hydrochloride 5 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 1 package NDC, 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?
Proficient Rx LP, NDC labeler code 82804. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
NebivololNebivolol 20 mg/1TabletOralMajor Pharmaceuticals0904-750000904-7500-04
NebivololNebivolol hydrochloride 5 mg/1TabletOralREMEDYREPACK INC.70518-464870518-4648-00
NebivololNebivolol hydrochloride 2.5 mg/1TabletOralNorthStar RxLLC72603-87072603-0870-01
NebivololNebivolol hydrochloride 5 mg/1TabletOralNorthStar RxLLC72603-87172603-0871-0172603-0871-02
NebivololNebivolol hydrochloride 10 mg/1TabletOralNorthStar RxLLC72603-87272603-0872-0172603-0872-02
NebivololNebivolol hydrochloride 20 mg/1TabletOralNorthStar RxLLC72603-87372603-0873-0172603-0873-02
NebivololNebivolol 2.5 mg/1TabletOralMajor Pharmaceuticals0904-749700904-7497-04
NebivololNebivolol 5 mg/1TabletOralMajor Pharmaceuticals0904-749800904-7498-04
NebivololNebivolol 10 mg/1TabletOralMajor Pharmaceuticals0904-749900904-7499-04
NebivololNebivolol hydrochloride 2.5 mg/1TabletOralMacleods Pharmaceuticals Limited33342-45733342-0457-0733342-0457-1033342-0457-25

All 90 Nebivolol NDCs

Other NDCs under ANDA 203825

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

FDA NDC Directory listings under ANDA 203825
ProductStrengthForm · routeLabelerProduct NDC
NebivololNebivolol hydrochloride 2.5 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-585
NebivololNebivolol hydrochloride 5 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-586
NebivololNebivolol hydrochloride 10 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-587
NebivololNebivolol hydrochloride 20 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-588
NebivololNebivolol hydrochloride 5 mg/1TabletOralBryant Ranch Prepack63629-4693
NebivololNebivolol hydrochloride 5 mg/1TabletOralBryant Ranch Prepack71335-2646

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