NDC Package 0245-0410-50 Hydrocodone Bitartrate 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:
0245-0410-50
Package Description:
500 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Hydrocodone Bitartrate And Acetaminophen
Non-Proprietary Name:
Hydrocodone Bitartrate And Acetaminophen
Substance Name:
Acetaminophen; Hydrocodone Bitartrate
Usage Information:
Hydrocodone bitartrate and acetaminophen tablets are 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:
00245041050
NDC to RxNorm Crosswalk:
  • RxCUI: 856999 - HYDROcodone bitartrate 10 MG / acetaminophen 325 MG Oral Tablet
  • RxCUI: 856999 - acetaminophen 325 MG / hydrocodone bitartrate 10 MG Oral Tablet
  • RxCUI: 856999 - APAP 325 MG / hydrocodone bitartrate 10 MG Oral Tablet
  • RxCUI: 857002 - HYDROcodone bitartrate 5 MG / acetaminophen 325 MG Oral Tablet
  • RxCUI: 857002 - acetaminophen 325 MG / hydrocodone bitartrate 5 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Upsher-smith Laboratories, Llc
    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:
    ANDA206484
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    03-27-2017
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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
    0245-0410-01100 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK (0245-0410-89)
    0245-0410-11100 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0245-0410-50?

    The NDC Packaged Code 0245-0410-50 is assigned to a package of 500 tablet in 1 bottle of Hydrocodone Bitartrate And Acetaminophen, a human prescription drug labeled by Upsher-smith Laboratories, Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 0245-0410 included in the NDC Directory?

    Yes, Hydrocodone Bitartrate And Acetaminophen with product code 0245-0410 is active and included in the NDC Directory. The product was first marketed by Upsher-smith Laboratories, Llc on March 27, 2017 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 0245-0410-50?

    The 11-digit format is 00245041050. 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 4-4-2 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
    4-4-20245-0410-505-4-200245-0410-50