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  5. NDC Package Code: 64725-0304-1 Chlorpromazine Hydrochloride

NDC Package 64725-0304-1 Chlorpromazine Hydrochloride

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:
64725-0304-1
Package Description:
100 TABLET, SUGAR COATED in 1 BOTTLE
Product Code:
64725-0304
Proprietary Name:
Chlorpromazine Hydrochloride
Usage Information:
For the management of manifestations of psychotic disorders. For the treatment of schizophrenia. To control nausea and vomiting. For relief of restlessness and apprehension before surgery. For acute intermittent porphyria. As an adjunct in the treatment of tetanus. To control the manifestations of the manic type of manic-depressive illness. For relief of intractable hiccups. For the treatment of severe behavioral problems in children (1 to 12 years of age) marked by combativeness and/or explosive hyperexcitable behavior (out of proportion to immediate provocations), and in the short-term treatment of hyperactive children who show excessive motor activity with accompanying conduct disorders consisting of some or all of the following symptoms: impulsivity, difficulty sustaining attention, aggressivity, mood lability and poor frustration tolerance.
11-Digit NDC Billing Format:
64725030401
NDC to RxNorm Crosswalk:
  • RxCUI: 991188 - chlorproMAZINE HCl 200 MG Oral Tablet
  • RxCUI: 991188 - chlorpromazine hydrochloride 200 MG Oral Tablet
    • Labeler Name:
    Tya Pharmaceuticals
    Sample Package:
    No
    Start Marketing Date:
    08-03-2011
    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 64725-0304-1?

    The NDC Packaged Code 64725-0304-1 is assigned to a package of 100 tablet, sugar coated in 1 bottle of Chlorpromazine Hydrochloride, labeled by Tya Pharmaceuticals. The product's dosage form is and is administered via form.

    Is NDC 64725-0304 included in the NDC Directory?

    No, Chlorpromazine Hydrochloride with product code 64725-0304 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 03, 2011 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 64725-0304-1?

    The 11-digit format is 64725030401. 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
    5-4-164725-0304-15-4-264725-0304-01