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  5. NDC Package Code: 69263-821-01 Pro-c-dure 6 Kit

NDC Package 69263-821-01 Pro-c-dure 6 Kit

Kenalog Kit Intra-articular; Intramuscular - 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:
69263-821-01
Package Description:
1 KIT in 1 CARTON * 1 VIAL in 1 CARTON (70121-1049-2) / 1 mL in 1 VIAL
Product Code:
69263-821
Proprietary Name:
Pro-c-dure 6 Kit
Non-Proprietary Name:
Kenalog
Usage Information:
Kenalog-40 Injection is contraindicated in patients who are hypersensitive to any components of this product (see WARNINGS: General). Intramuscular corticosteroid preparations are contraindicated for idiopathic thrombocytopenic purpura.
11-Digit NDC Billing Format:
69263082101
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 1792144 - triamcinolone acetonide 40 MG in 1 ML Injection
  • RxCUI: 1792144 - 1 ML triamcinolone acetonide 40 MG/ML Injection
  • RxCUI: 1792144 - triamcinolone acetonide 40 MG per 1 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Oaklock, Llc
    Dosage Form:
    Kit - A packaged collection of related material.
    Administration Route(s):
  • Intra-articular - Administration within a joint.
  • Intramuscular - Administration within a muscle.
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    08-17-2015
    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 69263-821-01?

    The NDC Packaged Code 69263-821-01 is assigned to a package of 1 kit in 1 carton * 1 vial in 1 carton (70121-1049-2) / 1 ml in 1 vial of Pro-c-dure 6 Kit, a human prescription drug labeled by Oaklock, Llc. The product's dosage form is kit and is administered via intra-articular; intramuscular form.

    Is NDC 69263-821 included in the NDC Directory?

    Yes, Pro-c-dure 6 Kit with product code 69263-821 is active and included in the NDC Directory. The product was first marketed by Oaklock, Llc on August 17, 2015 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 69263-821-01?

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

    What is the 11-digit format for NDC 69263-821-01?

    The 11-digit format is 69263082101. 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
    5-3-269263-821-015-4-269263-0821-01