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  5. NDC Package Code: 64725-2435-1 Benztropine Mesylate

NDC Package 64725-2435-1 Benztropine Mesylate

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
64725-2435-1
Package Description:
30 TABLET in 1 CONTAINER
Product Code:
64725-2435
Proprietary Name:
Benztropine Mesylate
Usage Information:
Benztropine is used to treat symptoms of Parkinson's disease or involuntary movements due to the side effects of certain psychiatric drugs (antipsychotics such as chlorpromazine/haloperidol). Benztropine belongs to a class of medication called anticholinergics that work by blocking a certain natural substance (acetylcholine). This helps decrease muscle stiffness, sweating, and the production of saliva, and helps improve walking ability in people with Parkinson's disease. Anticholinergics can stop severe muscle spasms of the back, neck, and eyes that are sometimes caused by psychiatric drugs. It can also decrease other side effects such as muscle stiffness/rigidity (extrapyramidal signs-EPS). It is not helpful in treating movement problems caused by tardive dyskinesia and may worsen them. Benztropine should not be used by children younger than 3 years.
11-Digit NDC Billing Format:
64725243501
NDC to RxNorm Crosswalk:
  • RxCUI: 885209 - benztropine mesylate 2 MG Oral Tablet
  • RxCUI: 885213 - benztropine mesylate 1 MG Oral Tablet
    • Labeler Name:
    Tya Pharmaceuticals
    Sample Package:
    No
    Start Marketing Date:
    08-27-2007
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    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 64725-2435-1?

    The NDC Packaged Code 64725-2435-1 is assigned to a package of 30 tablet in 1 container of Benztropine Mesylate, labeled by Tya Pharmaceuticals. The product's dosage form is and is administered via form.

    Is NDC 64725-2435 included in the NDC Directory?

    No, Benztropine Mesylate with product code 64725-2435 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Tya Pharmaceuticals on August 27, 2007 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 64725-2435-1?

    The 11-digit format is 64725243501. 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
    5-4-164725-2435-15-4-264725-2435-01