What is NDC 31722-588?

31722-588 is the product NDC for Nebivolol, Nebivolol hydrochloride 20 mg/1 tablet, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.

Camber Pharmaceuticals, Inc., NDC labeler code 31722. 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 31722-588 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)31722-588Labeler and product segments. Claims need a package NDC.

Product NDC at billing width31722-0588Add 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
31722-588-01	3172205880131722058801	100 TABLET in 1 BOTTLE (31722-588-01)Marketed from Sep 17, 2021
31722-588-30	3172205883031722058830	30 TABLET in 1 BOTTLE (31722-588-30)Marketed from Sep 17, 2021
31722-588-32	3172205883231722058832	10 BLISTER PACK in 1 CARTON (31722-588-32) / 10 TABLET in 1 BLISTER PACK (31722-588-31)Marketed from Sep 17, 2021
31722-588-34	3172205883431722058834	18 BLISTER PACK in 1 CARTON (31722-588-34) / 7 TABLET in 1 BLISTER PACK (31722-588-33)Marketed from Sep 17, 2021
31722-588-90	3172205889031722058890	90 TABLET in 1 BOTTLE (31722-588-90)Marketed from Sep 17, 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: Camber Pharmaceuticals, Inc.NDC labeler code 31722
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203825
Marketing start: Sep 17, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic beta-Antagonists (Mechanism)
Identifiers: Product ID 31722-588_103af555-44dd-5dfb-e063-6294a90a259fSPL ID 103af555-44dd-5dfb-e063-6294a90a259fSPL set ID 202d5142-6180-4d48-9a9f-1bd6992fc49bRxCUI 387013, 751612, 751618, 827073UNII JGS34J7L9IUPC 0331722585309, 0331722588300, 0331722587303, 0331722586306
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

N431722058801 followed by a unit qualifier and the quantity

Package 31722-0588-01. 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 Jan 31, 2024.

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 31722-588

What is NDC 31722-588?: 31722-588 is the product NDC for Nebivolol, Nebivolol hydrochloride 20 mg/1 tablet, listed with the FDA by Camber Pharmaceuticals, Inc.. It has 5 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?: Camber Pharmaceuticals, Inc., NDC labeler code 31722. 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 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
Product	Strength	Form · route	Labeler	Product NDC
Nebivolol	Nebivolol hydrochloride 2.5 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-585
Nebivolol	Nebivolol hydrochloride 5 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-586
Nebivolol	Nebivolol hydrochloride 10 mg/1	TabletOral	Camber Pharmaceuticals, Inc.	31722-587
Nebivolol	Nebivolol hydrochloride 5 mg/1	TabletOral	Bryant Ranch Prepack	63629-4693
Nebivolol	Nebivolol hydrochloride 5 mg/1	TabletOral	Bryant Ranch Prepack	71335-2646
Nebivolol	Nebivolol hydrochloride 5 mg/1	TabletOral	Proficient Rx LP	82804-120