NDC Package 70518-2409-2 Trihexyphenidyl Hydrochloride

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:
70518-2409-2
Package Description:
100 POUCH in 1 BOX / 1 TABLET in 1 POUCH (70518-2409-3)
Product Code:
Proprietary Name:
Trihexyphenidyl Hydrochloride
Non-Proprietary Name:
Trihexyphenidyl Hydrochloride
Substance Name:
Trihexyphenidyl Hydrochloride
Usage Information:
This drug is indicated as an adjunct in the treatment of all forms of parkinsonism (postencephalitic, arteriosclerotic, and idiopathic). It is often useful as adjuvant therapy when treating these forms of parkinsonism with levodopa. Additionally, it is indicated for the control of extrapyramidal disorders caused by central nervous system drugs such as the dibenzoxazepines, phenothiazines, thioxanthenes, and butyrophenones.
11-Digit NDC Billing Format:
70518240902
NDC to RxNorm Crosswalk:
  • RxCUI: 905283 - trihexyphenidyl HCl 5 MG Oral Tablet
  • RxCUI: 905283 - trihexyphenidyl hydrochloride 5 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Remedyrepack Inc.
    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.
  • Sample Package:
    No
    FDA Application Number:
    ANDA040254
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    11-08-2019
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    70518-2409-430 TABLET in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70518-2409-2?

    The NDC Packaged Code 70518-2409-2 is assigned to a package of 100 pouch in 1 box / 1 tablet in 1 pouch (70518-2409-3) of Trihexyphenidyl Hydrochloride, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 70518-2409 included in the NDC Directory?

    Yes, Trihexyphenidyl Hydrochloride with product code 70518-2409 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on November 08, 2019 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 70518-2409-2?

    The 11-digit format is 70518240902. 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
    5-4-170518-2409-25-4-270518-2409-02