NDC Package 63187-363-20 Oxycodone And Acetaminophen

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

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:
63187-363-20
Package Description:
20 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Oxycodone And Acetaminophen
Non-Proprietary Name:
Oxycodone And Acetaminophen
Substance Name:
Acetaminophen; Oxycodone Hydrochloride
Usage Information:
Oxycodone and Acetaminophen Tablets is indicated for the relief of moderate to moderately severe pain.
11-Digit NDC Billing Format:
63187036320
NDC to RxNorm Crosswalk:
  • RxCUI: 1049214 - oxyCODONE 10 MG / acetaminophen 325 MG Oral Tablet
  • RxCUI: 1049214 - acetaminophen 325 MG / oxycodone hydrochloride 10 MG Oral Tablet
  • RxCUI: 1049214 - APAP 325 MG / oxycodone hydrochloride 10 MG Oral Tablet
  • RxCUI: 1049221 - oxyCODONE 5 MG / acetaminophen 325 MG Oral Tablet
  • RxCUI: 1049221 - acetaminophen 325 MG / oxycodone hydrochloride 5 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Proficient Rx Lp
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • DEA Schedule:
    Schedule II (CII) Substances
    Sample Package:
    No
    FDA Application Number:
    ANDA202677
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    01-17-2012
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    63187-363-1212 TABLET in 1 BOTTLE
    63187-363-1515 TABLET in 1 BOTTLE
    63187-363-3030 TABLET in 1 BOTTLE
    63187-363-6060 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 63187-363-20?

    The NDC Packaged Code 63187-363-20 is assigned to a package of 20 tablet in 1 bottle of Oxycodone And Acetaminophen, a human prescription drug labeled by Proficient Rx Lp. The product's dosage form is tablet and is administered via oral form.

    Is NDC 63187-363 included in the NDC Directory?

    Yes, Oxycodone And Acetaminophen with product code 63187-363 is active and included in the NDC Directory. The product was first marketed by Proficient Rx Lp on January 17, 2012 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 63187-363-20?

    The 11-digit format is 63187036320. 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
    5-3-263187-363-205-4-263187-0363-20