NDC Package 64950-342-47 Hycodan

Hydrocodone Bitartrate And Homatropine Methylbromide Solution 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:
64950-342-47
Package Description:
473 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Hycodan
Non-Proprietary Name:
Hydrocodone Bitartrate And Homatropine Methylbromide
Substance Name:
Homatropine Methylbromide; Hydrocodone Bitartrate
Usage Information:
HYCODAN is indicated for the symptomatic relief of cough in patients 18 years of age and older.
11-Digit NDC Billing Format:
64950034247
NDC to RxNorm Crosswalk:
  • RxCUI: 992656 - HYDROcodone bitartrate 5 MG / homatropine methylbromide 1.5 MG Oral Tablet
  • RxCUI: 992656 - homatropine methylbromide 1.5 MG / hydrocodone bitartrate 5 MG Oral Tablet
  • RxCUI: 992660 - Hycodan 5 MG / 1.5 MG Oral Tablet
  • RxCUI: 992660 - homatropine methylbromide 1.5 MG / hydrocodone bitartrate 5 MG Oral Tablet [Hycodan]
  • RxCUI: 992660 - Hycodan (homatropine methylbromide 1.5 MG / hydrocodone bitartrate 5 MG) Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Genus Lifesciences Inc.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • DEA Schedule:
    Schedule II (CII) Substances
    Sample Package:
    No
    FDA Application Number:
    NDA005213
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    06-10-2019
    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
    64950-342-4540 CUP, UNIT-DOSE in 1 CASE / 5 mL in 1 CUP, UNIT-DOSE (64950-342-05)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 64950-342-47?

    The NDC Packaged Code 64950-342-47 is assigned to a package of 473 ml in 1 bottle of Hycodan, a human prescription drug labeled by Genus Lifesciences Inc.. The product's dosage form is solution and is administered via oral form.

    Is NDC 64950-342 included in the NDC Directory?

    Yes, Hycodan with product code 64950-342 is active and included in the NDC Directory. The product was first marketed by Genus Lifesciences Inc. on June 10, 2019 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 64950-342-47?

    The 11-digit format is 64950034247. 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
    5-3-264950-342-475-4-264950-0342-47