NDC Package 54868-2571-0 Imipramine Hydrochloride

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory .

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:
54868-2571-0
Package Description:
30 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Imipramine Hydrochloride
Usage Information:
The concomitant use of monoamine oxidase inhibiting compounds is contraindicated. Hyperpyretic crises or severe convulsive seizures may occur in patients receiving such combinations. The potentiation of adverse effects can be serious, or even fatal. When it is desired to substitute imipramine hydrochloride tablets in patients receiving a monoamine oxidase inhibitor, as long an interval should elapse as the clinical situation will allow, with a minimum of 14 days. Initial dosage should be low and increases should be gradual and cautiously prescribed.The drug is contraindicated during the acute recovery period after a myocardial infarction. Patients with a known hypersensitivity to this compound should not be given the drug. The possibility of cross-sensitivity to other dibenzazepine compounds should be kept in mind.
11-Digit NDC Billing Format:
54868257100
NDC to RxNorm Crosswalk:
  • RxCUI: 835564 - imipramine HCl 25 MG Oral Tablet
  • RxCUI: 835564 - imipramine hydrochloride 25 MG Oral Tablet
  • RxCUI: 835568 - imipramine HCl 50 MG Oral Tablet
  • RxCUI: 835568 - imipramine hydrochloride 50 MG Oral Tablet
  • RxCUI: 835593 - imipramine HCl 10 MG Oral Tablet
  • Labeler Name:
    Physicians Total Care, Inc.
    Sample Package:
    No
    FDA Application Number:
    ANDA090443
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    04-14-2003
    End Marketing Date:
    06-30-2006
    Listing Expiration Date:
    06-30-2006
    Exclude Flag:
    D
    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
    54868-2571-160 TABLET, FILM COATED in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 54868-2571-0?

    The NDC Packaged Code 54868-2571-0 is assigned to a package of 30 tablet, film coated in 1 bottle of Imipramine Hydrochloride, labeled by Physicians Total Care, Inc.. The product's dosage form is and is administered via form.

    Is NDC 54868-2571 included in the NDC Directory?

    The product was first marketed by Physicians Total Care, Inc. on April 14, 2003 and its listing in the NDC Directory is set to expire on June 30, 2006 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 54868-2571-0?

    The 11-digit format is 54868257100. 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
    5-4-154868-2571-05-4-254868-2571-00