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  5. NDC Package Code: 82228-712-28 Attruby

NDC Package 82228-712-28 Attruby

Acoramidis Hydrochloride Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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:
82228-712-28
Package Description:
4 DOSE PACK in 1 CARTON / 1 BLISTER PACK in 1 DOSE PACK / 28 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
82228-712
Proprietary Name:
Attruby
Non-Proprietary Name:
Acoramidis Hydrochloride
Substance Name:
Acoramidis Hydrochloride
Usage Information:
ATTRUBY is indicated for the treatment of the cardiomyopathy of wild-type or variant transthyretin-mediated amyloidosis (ATTR-CM) in adults to reduce cardiovascular death and cardiovascular-related hospitalization.
11-Digit NDC Billing Format:
82228071228
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
4 EA
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Bridgebio Pharma, Inc.
Dosage Form:
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
ACORAMIDIS HYDROCHLORIDE 356 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
NDA216540
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
11-22-2024
Listing Expiration Date:
12-31-2026
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 82228-712-28?

The NDC Packaged Code 82228-712-28 is assigned to a package of 4 dose pack in 1 carton / 1 blister pack in 1 dose pack / 28 tablet, film coated in 1 blister pack of Attruby, a human prescription drug labeled by Bridgebio Pharma, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 4 billable units per package.

Is NDC 82228-712 included in the NDC Directory?

Yes, Attruby with product code 82228-712 is active and included in the NDC Directory. The product was first marketed by Bridgebio Pharma, Inc. on November 22, 2024 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 82228-712-28?

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 4.

What is the 11-digit format for NDC 82228-712-28?

The 11-digit format is 82228071228. 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 5-3-2 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
5-3-282228-712-285-4-282228-0712-28