NDC Package 58437-018-00 Sumatriptan

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

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
58437-018-00
Package Description:
432 BLISTER PACK in 1 CASE / 9 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
Non-Proprietary Name:
Sumatriptan
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:
58437001800
Product Type:
Drug For Further Processing
Labeler Name:
Glaxosmithkline Llc
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.
Active Ingredient(s):
Sample Package:
N/A
Marketing Category:
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date:
01-01-2020
Listing Expiration Date:
12-31-2025
Exclude Flag:
N
Unfinished Product:
Yes
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 58437-018-00?

The NDC Packaged Code 58437-018-00 is assigned to an UNFINISHED drug package of 432 blister pack in 1 case / 9 tablet, film coated in 1 blister pack of Sumatriptan, drug for further processing labeled by Glaxosmithkline Llc. The product's dosage form is tablet, film coated and is administered via form.

Is NDC 58437-018 included in the NDC Directory?

Yes, Sumatriptan is an UNFINISHED PRODUCT with code 58437-018 that is active and included in the NDC Directory. The product was first marketed by Glaxosmithkline Llc on January 01, 2020 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 58437-018-00?

The 11-digit format is 58437001800. 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
5-3-258437-018-005-4-258437-0018-00