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  5. NDC Package Code: 70518-1793-1 Imipramine Hydrochloride

NDC Package 70518-1793-1 Imipramine Hydrochloride

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
70518-1793-1
Package Description:
30 TABLET in 1 BLISTER PACK
Product Code:
70518-1793
Proprietary Name:
Imipramine Hydrochloride
Non-Proprietary Name:
Imipramine Hydrochloride
Substance Name:
Imipramine Hydrochloride
Usage Information:
Depression:For the relief of symptoms of depression. Endogenous depression is more likely to be alleviated than other depressive states. One to three weeks of treatment may be needed before optimal therapeutic effects are evident. Childhood Enuresis: May be useful as temporary adjunctive therapy in reducing enuresis in children aged 6 years and older, after possible organic causes have been excludedby appropriate tests. In patients having daytime symptoms of frequency and urgency, examination should include voiding cystourethrography and cystoscopy, as necessary. The effectiveness of treatment may decrease with continued drug administration.
11-Digit NDC Billing Format:
70518179301
NDC to RxNorm Crosswalk:
  • RxCUI: 835564 - imipramine HCl 25 MG Oral Tablet
  • RxCUI: 835564 - imipramine hydrochloride 25 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.
    • Active Ingredient(s):
  • IMIPRAMINE HYDROCHLORIDE 25 mg/1
    • Pharmacologic Class(es):
  • Tricyclic Antidepressant - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA088262
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    01-11-2019
    End Marketing Date:
    08-31-2024
    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.

    Frequently Asked Questions

    What is NDC 70518-1793-1?

    The NDC Packaged Code 70518-1793-1 is assigned to a package of 30 tablet in 1 blister pack of Imipramine Hydrochloride, a human prescription drug labeled by Remedyrepack Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 70518-1793 included in the NDC Directory?

    Yes, Imipramine Hydrochloride with product code 70518-1793 is active and included in the NDC Directory. The product was first marketed by Remedyrepack Inc. on January 11, 2019.

    What is the 11-digit format for NDC 70518-1793-1?

    The 11-digit format is 70518179301. 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
    5-4-170518-1793-15-4-270518-1793-01