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  5. NDC Package Code: 64950-901-10 Oxycodone Hydrochloride

NDC Package 64950-901-10 Oxycodone Hydrochloride

Capsule 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:
64950-901-10
Package Description:
100 CAPSULE in 1 BOTTLE, PLASTIC
Product Code:
64950-901
Proprietary Name:
Oxycodone Hydrochloride
Non-Proprietary Name:
Oxycodone Hydrochloride
Substance Name:
Oxycodone Hydrochloride
Usage Information:
Oxycodone Hydrochloride Capsule is an opioid agonist indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate.
11-Digit NDC Billing Format:
64950090110
NDC to RxNorm Crosswalk:
  • RxCUI: 1049696 - oxyCODONE HCl 5 MG Oral Capsule
  • RxCUI: 1049696 - oxycodone hydrochloride 5 MG Oral Capsule
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Genus Lifesciences Inc.
    Dosage Form:
    Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • OXYCODONE HYDROCHLORIDE 5 mg/1
    • Pharmacologic Class(es):
  • Full Opioid Agonists - [MoA] (Mechanism of Action)
  • Opioid Agonist - [EPC] (Established Pharmacologic Class)
    • DEA Schedule:
    Schedule II (CII) Substances
    Sample Package:
    No
    FDA Application Number:
    NDA200534
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    10-20-2010
    Listing Expiration Date:
    12-31-2025
    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 64950-901-10?

    The NDC Packaged Code 64950-901-10 is assigned to a package of 100 capsule in 1 bottle, plastic of Oxycodone Hydrochloride, a human prescription drug labeled by Genus Lifesciences Inc.. The product's dosage form is capsule and is administered via oral form.

    Is NDC 64950-901 included in the NDC Directory?

    Yes, Oxycodone Hydrochloride with product code 64950-901 is active and included in the NDC Directory. The product was first marketed by Genus Lifesciences Inc. on October 20, 2010 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 64950-901-10?

    The 11-digit format is 64950090110. 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
    5-3-264950-901-105-4-264950-0901-10