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  5. NDC Package Code: 69945-602-20 Sodium Iodide I 123

NDC Package 69945-602-20 Sodium Iodide I 123

Capsule, Gelatin 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:
69945-602-20
Package Description:
1 BOTTLE in 1 CAN / 1 CAPSULE, GELATIN COATED in 1 BOTTLE
Product Code:
69945-602
Proprietary Name:
Sodium Iodide I 123
Non-Proprietary Name:
Sodium Iodide I 123
Substance Name:
Sodium Iodide I-123
Usage Information:
Administration of Sodium Iodide I 123 Capsules is indicated as a diagnostic procedure to be used in evaluating thyroid function and/or morphology.
11-Digit NDC Billing Format:
69945060220
Product Type:
Human Prescription Drug
Labeler Name:
Curium Us Llc
Dosage Form:
Capsule, Gelatin Coated - A solid dosage form in which the drug is enclosed within either a hard or soft soluble container made from a suitable form of gelatin; through a banding process, the capsule is coated with additional layers of gelatin so as to form a complete seal.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • SODIUM IODIDE I-123 200 uCi/1
    • Sample Package:
    No
    FDA Application Number:
    ANDA071910
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-11-2007
    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 69945-602-20?

    The NDC Packaged Code 69945-602-20 is assigned to a package of 1 bottle in 1 can / 1 capsule, gelatin coated in 1 bottle of Sodium Iodide I 123, a human prescription drug labeled by Curium Us Llc. The product's dosage form is capsule, gelatin coated and is administered via oral form.

    Is NDC 69945-602 included in the NDC Directory?

    Yes, Sodium Iodide I 123 with product code 69945-602 is active and included in the NDC Directory. The product was first marketed by Curium Us Llc on April 11, 2007 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 11-digit format for NDC 69945-602-20?

    The 11-digit format is 69945060220. 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
    5-3-269945-602-205-4-269945-0602-20