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  5. NDC Package Code: 70771-1697-1 Prochlorperazine Maleate

NDC Package 70771-1697-1 Prochlorperazine Maleate

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:
70771-1697-1
Package Description:
100 TABLET in 1 BOTTLE
Product Code:
70771-1697
Proprietary Name:
Prochlorperazine Maleate
Non-Proprietary Name:
Prochlorperazine Maleate
Substance Name:
Prochlorperazine Maleate
Usage Information:
This medication is used to treat severe nausea and vomiting from certain causes (for example, after surgery or cancer treatment). Prochlorperazine belongs to a class of drugs known as phenothiazines. This medication is not recommended for use in children younger than 2 years or in children going through surgery.
11-Digit NDC Billing Format:
70771169701
NDC to RxNorm Crosswalk:
  • RxCUI: 198365 - prochlorperazine maleate 10 MG Oral Tablet
  • RxCUI: 198365 - prochlorperazine 10 MG Oral Tablet
  • RxCUI: 198365 - prochlorperazine (as prochlorperazine maleate) 10 MG Oral Tablet
  • RxCUI: 312635 - prochlorperazine maleate 5 MG Oral Tablet
  • RxCUI: 312635 - prochlorperazine 5 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Zydus Lifesciences Limited
    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):
  • PROCHLORPERAZINE MALEATE 5 mg/1
    • Pharmacologic Class(es):
  • Phenothiazine - [EPC] (Established Pharmacologic Class)
  • Phenothiazines - [CS]
    • Sample Package:
    No
    FDA Application Number:
    ANDA216495
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-10-2022
    Listing Expiration Date:
    12-31-2024
    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 70771-1697-1?

    The NDC Packaged Code 70771-1697-1 is assigned to a package of 100 tablet in 1 bottle of Prochlorperazine Maleate, a human prescription drug labeled by Zydus Lifesciences Limited. The product's dosage form is tablet and is administered via oral form.

    Is NDC 70771-1697 included in the NDC Directory?

    Yes, Prochlorperazine Maleate with product code 70771-1697 is active and included in the NDC Directory. The product was first marketed by Zydus Lifesciences Limited on August 10, 2022 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70771-1697-1?

    The 11-digit format is 70771169701. 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
    5-4-170771-1697-15-4-270771-1697-01