NDC Package 0487-9701-30 Budesonide

Inhalant Respiratory (inhalation) - View Billable Units, 11-Digit Format, RxNorm

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:
0487-9701-30
Package Description:
30 POUCH in 1 CARTON / 1 AMPULE in 1 POUCH / 2 mL in 1 AMPULE
Product Code:
Proprietary Name:
Budesonide
Non-Proprietary Name:
Budesonide
Substance Name:
Budesonide
Usage Information:
Budesonide is used to control and prevent symptoms (wheezing and shortness of breath) caused by asthma. This medication belongs to a class of drugs known as corticosteroids. It works directly in the lungs to make breathing easier by reducing the irritation and swelling of the airways. This medication must be used regularly to be effective. It does not work right away and should not be used to relieve sudden asthma attacks. If an asthma attack occurs, use your quick-relief inhaler as prescribed.
11-Digit NDC Billing Format:
00487970130
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 349094 - budesonide 0.25 MG in 2 ML Inhalation Suspension
  • RxCUI: 349094 - budesonide 0.125 MG/ML Inhalation Suspension
  • RxCUI: 349094 - budesonide 0.25 MG per 2 ML Inhalation Suspension
  • RxCUI: 351109 - budesonide 0.5 MG in 2 ML Inhalation Suspension
  • RxCUI: 351109 - budesonide 0.25 MG/ML Inhalation Suspension
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Nephron Pharmaceuticals Corporation
    Dosage Form:
    Inhalant - A special class of inhalations consisting of a drug or combination of drugs, that by virtue of their high vapor pressure can be carried by an air current into the nasal passage where they exert their effect; the container from which the inhalant generally is administered is known as an inhaler.
    Administration Route(s):
  • Respiratory (inhalation) - Administration within the respiratory tract by inhaling orally or nasally for local or systemic effect.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA078202
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-01-2013
    Listing Expiration Date:
    12-31-2024
    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.

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    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 0487-9701-30 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    00487970130J7626Budesonide non-comp unitUP TO 0.50 MG230130

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    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0487-9701-016 POUCH in 1 CARTON / 5 AMPULE in 1 POUCH / 2 mL in 1 AMPULE

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    Frequently Asked Questions

    What is NDC 0487-9701-30?

    The NDC Packaged Code 0487-9701-30 is assigned to a package of 30 pouch in 1 carton / 1 ampule in 1 pouch / 2 ml in 1 ampule of Budesonide, a human prescription drug labeled by Nephron Pharmaceuticals Corporation. The product's dosage form is inhalant and is administered via respiratory (inhalation) form.

    Is NDC 0487-9701 included in the NDC Directory?

    Yes, Budesonide with product code 0487-9701 is active and included in the NDC Directory. The product was first marketed by Nephron Pharmaceuticals Corporation on October 01, 2013 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 0487-9701-30?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 0487-9701-30?

    The 11-digit format is 00487970130. 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
    4-4-20487-9701-305-4-200487-9701-30