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  5. NDC Package Code: 59212-702-12 Orapred Odt

NDC Package 59212-702-12 Orapred Odt

Prednisolone Sodium Phosphate Tablet, Orally Disintegrating 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:
59212-702-12
Package Description:
2 BLISTER PACK in 1 CARTON / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (59212-702-06)
Product Code:
59212-702
Proprietary Name:
Orapred Odt
Non-Proprietary Name:
Prednisolone Sodium Phosphate
Substance Name:
Prednisolone Sodium Phosphate
Usage Information:
Prednisolone is used to treat conditions such as arthritis, blood disorders, severe allergic reactions, certain cancers, eye conditions, skin/kidney/intestinal/lung diseases, and immune system disorders. It decreases your immune system's response to various diseases to reduce symptoms such as swelling, pain and allergic-type reactions. This medication is a corticosteroid hormone. Prednisolone may also be used with other medications in hormone disorders.
11-Digit NDC Billing Format:
59212070212
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
2 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 643123 - prednisoLONE sodium phosphate 10 MG Disintegrating Oral Tablet
  • RxCUI: 643123 - prednisolone 10 MG Disintegrating Oral Tablet
  • RxCUI: 643123 - prednisolone 10 MG (prednisolone sodium phosphate 13.4 MG) Disintegrating Oral Tablet
  • RxCUI: 643125 - prednisoLONE sodium phosphate 15 MG Disintegrating Oral Tablet
  • RxCUI: 643125 - prednisolone 15 MG Disintegrating Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Concordia Pharmaceuticals Inc.
    Dosage Form:
    Tablet, Orally Disintegrating - A solid dosage form containing medicinal substances which disintegrates rapidly, usually within a matter of seconds, when placed upon the tongue.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • PREDNISOLONE SODIUM PHOSPHATE 30 mg/1
    • Pharmacologic Class(es):
  • Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
  • Corticosteroid - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    NDA021959
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    06-01-2006
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 59212-702-12?

    The NDC Packaged Code 59212-702-12 is assigned to a package of 2 blister pack in 1 carton / 6 tablet, orally disintegrating in 1 blister pack (59212-702-06) of Orapred Odt, a human prescription drug labeled by Concordia Pharmaceuticals Inc.. The product's dosage form is tablet, orally disintegrating and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 2 billable units per package.

    Is NDC 59212-702 included in the NDC Directory?

    Yes, Orapred Odt with product code 59212-702 is active and included in the NDC Directory. The product was first marketed by Concordia Pharmaceuticals Inc. on June 01, 2006 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 59212-702-12?

    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 2.

    What is the 11-digit format for NDC 59212-702-12?

    The 11-digit format is 59212070212. 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
    5-3-259212-702-125-4-259212-0702-12