NDC Package 45802-598-06 Sumatriptan

Spray Nasal - View Billable Units, 11-Digit Format, RxNorm

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:
45802-598-06
Package Description:
6 CONTAINER in 1 CARTON / 1 SPRAY in 1 CONTAINER (45802-598-00)
Product Code:
Proprietary Name:
Sumatriptan
Non-Proprietary Name:
Sumatriptan
Substance Name:
Sumatriptan
Usage Information:
Sumatriptan 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. Sumatriptan 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. Sumatriptan does not prevent future migraines or lessen how often you get migraine attacks.
11-Digit NDC Billing Format:
45802059806
NDC to RxNorm Crosswalk:
  • RxCUI: 313159 - SUMAtriptan 5 MG/ACTUAT Nasal Spray
  • RxCUI: 313159 - sumatriptan 5 MG/ACTUAT Nasal Spray
  • RxCUI: 313159 - sumatriptan 5 MG/0.1 ML Nasal Spray
  • RxCUI: 314227 - SUMAtriptan 20 MG/ACTUAT Nasal Spray
  • RxCUI: 314227 - sumatriptan 20 MG/ACTUAT Nasal Spray
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Padagis Israel Pharmaceuticals Ltd
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    Administration Route(s):
  • Nasal - Administration to the nose; administered by way of the nose.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA213465
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-04-2020
    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 45802-598-06?

    The NDC Packaged Code 45802-598-06 is assigned to a package of 6 container in 1 carton / 1 spray in 1 container (45802-598-00) of Sumatriptan, a human prescription drug labeled by Padagis Israel Pharmaceuticals Ltd. The product's dosage form is spray and is administered via nasal form.

    Is NDC 45802-598 included in the NDC Directory?

    Yes, Sumatriptan with product code 45802-598 is active and included in the NDC Directory. The product was first marketed by Padagis Israel Pharmaceuticals Ltd on October 04, 2020 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 45802-598-06?

    The 11-digit format is 45802059806. 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 5-3-2 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
    5-3-245802-598-065-4-245802-0598-06