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  5. NDC Package Code: 70771-1107-0 Eletriptan Hydrobromide

NDC Package 70771-1107-0 Eletriptan Hydrobromide

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

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
70771-1107-0
Package Description:
1000 TABLET, FILM COATED in 1 BOTTLE
Product Code:
70771-1107
Proprietary Name:
Eletriptan Hydrobromide
Non-Proprietary Name:
Eletriptan Hydrobromide
Substance Name:
Eletriptan Hydrobromide
Usage Information:
Eletriptan is used to treat migraines. It helps to relieve headache, pain, and other migraine symptoms (including nausea, vomiting, sensitivity to light/sound). Prompt treatment helps you return to your normal routine and may decrease your need for other pain medications. Eletriptan belongs to a class of drugs known as triptans. It affects a certain natural substance (serotonin) that causes narrowing of blood vessels in the brain. It may also relieve pain by affecting certain nerves in the brain. Eletriptan does not prevent future migraines or lessen how often you get migraine attacks.
11-Digit NDC Billing Format:
70771110700
NDC to RxNorm Crosswalk:
  • RxCUI: 359493 - eletriptan HBr 20 MG Oral Tablet
  • RxCUI: 359493 - eletriptan 20 MG Oral Tablet
  • RxCUI: 359493 - eletriptan 20 MG (as eletriptan HBr 24.2 MG) Oral Tablet
  • RxCUI: 359494 - eletriptan HBr 40 MG Oral Tablet
  • RxCUI: 359494 - eletriptan 40 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Zydus Lifesciences Limited
    Dosage Form:
    Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ELETRIPTAN HYDROBROMIDE 20 mg/1
    • Pharmacologic Class(es):
  • Serotonin 1b Receptor Agonists - [MoA] (Mechanism of Action)
  • Serotonin 1d Receptor Agonists - [MoA] (Mechanism of Action)
  • Serotonin-1b and Serotonin-1d Receptor Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA206409
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-12-2017
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    70771-1107-330 TABLET, FILM COATED in 1 BOTTLE
    70771-1107-410 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1107-2)
    70771-1107-61 BLISTER PACK in 1 CARTON / 6 TABLET, FILM COATED in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70771-1107-0?

    The NDC Packaged Code 70771-1107-0 is assigned to a package of 1000 tablet, film coated in 1 bottle of Eletriptan Hydrobromide, a human prescription drug labeled by Zydus Lifesciences Limited. The product's dosage form is tablet, film coated and is administered via oral form.

    Is NDC 70771-1107 included in the NDC Directory?

    Yes, Eletriptan Hydrobromide with product code 70771-1107 is active and included in the NDC Directory. The product was first marketed by Zydus Lifesciences Limited on July 12, 2017 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 70771-1107-0?

    The 11-digit format is 70771110700. 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
    5-4-170771-1107-05-4-270771-1107-00