NDC Package 63187-969-09 Sumatriptan

Sumatriptan Succinate Tablet Oral - 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:
63187-969-09
Package Description:
1 BLISTER PACK in 1 CARTON / 9 TABLET in 1 BLISTER PACK
Product Code:
Proprietary Name:
Sumatriptan
Non-Proprietary Name:
Sumatriptan Succinate
Substance Name:
Sumatriptan Succinate
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:
63187096909
NDC to RxNorm Crosswalk:
  • RxCUI: 315223 - SUMAtriptan succinate 25 MG Oral Tablet
  • RxCUI: 315223 - sumatriptan 25 MG Oral Tablet
  • RxCUI: 315223 - sumatriptan 25 MG (as sumatriptan succinate 35 MG) Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Proficient Rx Lp
    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):
    Sample Package:
    No
    FDA Application Number:
    ANDA078327
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-17-2009
    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 63187-969-09?

    The NDC Packaged Code 63187-969-09 is assigned to a package of 1 blister pack in 1 carton / 9 tablet in 1 blister pack of Sumatriptan, a human prescription drug labeled by Proficient Rx Lp. The product's dosage form is tablet and is administered via oral form.

    Is NDC 63187-969 included in the NDC Directory?

    Yes, Sumatriptan with product code 63187-969 is active and included in the NDC Directory. The product was first marketed by Proficient Rx Lp on August 17, 2009 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 63187-969-09?

    The 11-digit format is 63187096909. 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
    5-3-263187-969-095-4-263187-0969-09