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  5. NDC Package Code: 17856-0390-2 Oxycodone Hydrochloride

NDC Package 17856-0390-2 Oxycodone Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
17856-0390-2
Package Description:
1 CUP, UNIT-DOSE in 1 CUP, UNIT-DOSE / 5 CUP, UNIT-DOSE in 1 CUP, UNIT-DOSE (17856-0390-3) / 72 CUP, UNIT-DOSE in 1 CUP, UNIT-DOSE (17856-0390-1) / 5 mL in 1 CUP, UNIT-DOSE
Product Code:
17856-0390
Proprietary Name:
Oxycodone Hydrochloride
Usage Information:
Oxycodone Hydrochloride Oral Solution is indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. Limitations of Use Because of the risks of addiction, abuse, and misuse with opioids, even at recommended doses [see Warnings and Precautions (5.2)], reserve Oxycodone Hydrochloride Oral Solution for use in patients for whom alternative treatment options [e.g., non-opioid analgesics or opioid combination products]:•Have not been tolerated, or are not expected to be tolerated,•Have not provided adequate analgesia, or are not expected to provide adequate analgesia.
11-Digit NDC Billing Format:
17856039002
NDC to RxNorm Crosswalk:
  • RxCUI: 1049604 - oxyCODONE HCl 5 MG in 5 mL Oral Solution
  • RxCUI: 1049604 - oxycodone hydrochloride 1 MG/ML Oral Solution
  • RxCUI: 1049604 - oxycodone hydrochloride 5 MG per 5 ML Oral Solution
    • Labeler Name:
    Atlantic Biologicals Corp.
    Sample Package:
    No
    Start Marketing Date:
    09-04-2014
    Listing Expiration Date:
    12-31-2023
    Exclude Flag:
    I
    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 17856-0390-2?

    The NDC Packaged Code 17856-0390-2 is assigned to a package of 1 cup, unit-dose in 1 cup, unit-dose / 5 cup, unit-dose in 1 cup, unit-dose (17856-0390-3) / 72 cup, unit-dose in 1 cup, unit-dose (17856-0390-1) / 5 ml in 1 cup, unit-dose of Oxycodone Hydrochloride, labeled by Atlantic Biologicals Corp.. The product's dosage form is and is administered via form.

    Is NDC 17856-0390 included in the NDC Directory?

    No, Oxycodone Hydrochloride with product code 17856-0390 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Atlantic Biologicals Corp. on September 04, 2014 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 17856-0390-2?

    The 11-digit format is 17856039002. 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 5-4-1 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
    5-4-117856-0390-25-4-217856-0390-02