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  5. NDC Package Code: 0904-7225-04 Nebivolol

NDC Package 0904-7225-04 Nebivolol

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0904-7225-04
Package Description:
30 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK
Product Code:
0904-7225
Proprietary Name:
Nebivolol
Non-Proprietary Name:
Nebivolol
Substance Name:
Nebivolol Hydrochloride
Usage Information:
Nebivolol is contraindicated in the following conditions:•Severe bradycardia•Heart block greater than first degree•Patients with cardiogenic shock•Decompensated cardiac failure•Sick sinus syndrome (unless a permanent pacemaker is in place)•Patients with severe hepatic impairment (Child-Pugh >B)•Patients who are hypersensitive to any component of this product.
11-Digit NDC Billing Format:
00904722504
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
30 EA
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Major Pharmaceuticals
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
NEBIVOLOL HYDROCHLORIDE 2.5 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA203966
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
03-02-2018
End Marketing Date:
08-31-2025
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0904-7225-04?

The NDC Packaged Code 0904-7225-04 is assigned to a package of 30 blister pack in 1 carton / 1 tablet in 1 blister pack of Nebivolol, a human prescription drug labeled by Major Pharmaceuticals. The product's dosage form is tablet and is administered via oral form.

Is NDC 0904-7225 included in the NDC Directory?

Yes, Nebivolol with product code 0904-7225 is active and included in the NDC Directory. The product was first marketed by Major Pharmaceuticals on March 02, 2018.

What is the NDC billing unit for package 0904-7225-04?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 30.

What is the 11-digit format for NDC 0904-7225-04?

The 11-digit format is 00904722504. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
4-4-20904-7225-045-4-200904-7225-04