What is NDC 67877-390?

67877-390 is the product NDC for Nebivolol, Nebivolol hydrochloride 20 mg/1 tablet, listed with the FDA by Ascend Laboratories, LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.

Ascend Laboratories, LLC, NDC labeler code 67877. 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 67877-390 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)67877-390Labeler and product segments. Claims need a package NDC.

Product NDC at billing width67877-0390Add 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
67877-390-01	6787703900167877039001	100 TABLET in 1 BOTTLE (67877-390-01)Marketed from Sep 16, 2021
67877-390-30	6787703903067877039030	30 TABLET in 1 BOTTLE (67877-390-30)Marketed from Sep 16, 2021
67877-390-33	6787703903367877039033	1 BLISTER PACK in 1 CARTON (67877-390-33) / 10 TABLET in 1 BLISTER PACKMarketed from Sep 16, 2021
67877-390-90	6787703909067877039090	90 TABLET in 1 BOTTLE (67877-390-90)Marketed from Sep 16, 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 — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Ascend Laboratories, LLCNDC labeler code 67877
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203828
Marketing start: Sep 16, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 67877-390_4f315a54-2598-4463-8884-0b643e86f8c0SPL ID 4f315a54-2598-4463-8884-0b643e86f8c0SPL set ID fecef8fc-b66b-4133-b66f-8d6b72750622RxCUI 387013, 751612, 751618, 827073UNII JGS34J7L9IUPC 0367877393308, 0367877391304, 0367877392905, 0367877390901
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

N467877039001 followed by a unit qualifier and the quantity

Package 67877-0390-01. 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

Current FDA label (SPL), effective Aug 14, 2025.

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 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 controlled trial…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67877-390

What is NDC 67877-390?: 67877-390 is the product NDC for Nebivolol, Nebivolol hydrochloride 20 mg/1 tablet, listed with the FDA by Ascend Laboratories, LLC. It has 4 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?: Ascend Laboratories, LLC, NDC labeler code 67877. 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 203828

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

FDA NDC Directory listings under ANDA 203828
Product	Strength	Form · route	Labeler	Product NDC
Nebivolol	Nebivolol hydrochloride 2.5 mg/1	TabletOral	A-S Medication Solutions	50090-5708
Nebivolol	Nebivolol hydrochloride 5 mg/1	TabletOral	A-S Medication Solutions	50090-5752
Nebivolol	Nebivolol hydrochloride 10 mg/1	TabletOral	A-S Medication Solutions	50090-5761
Nebivolol	Nebivolol hydrochloride 5 mg/1	TabletOral	American Health Packaging	60687-641
Nebivolol	Nebivolol hydrochloride 10 mg/1	TabletOral	American Health Packaging	60687-652
Nebivolol	Nebivolol hydrochloride 10 mg/1	TabletOral	Ascend Laboratories, LLC	67877-391
Nebivolol	Nebivolol hydrochloride 5 mg/1	TabletOral	Ascend Laboratories, LLC	67877-392
Nebivolol	Nebivolol hydrochloride 2.5 mg/1	TabletOral	Ascend Laboratories, LLC	67877-393
Nebivolol	Nebivolol hydrochloride 5 mg/1	TabletOral	REMEDYREPACK INC.	70518-3527