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NDC 51407-0012-09 Sumatriptan Succinate 50 mg/1 Details
Sumatriptan Succinate 50 mg/1
Sumatriptan Succinate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Golden State Medical Supply, Inc.. The primary component is SUMATRIPTAN SUCCINATE.
MedlinePlus Drug Summary
Sumatriptan is used to treat the symptoms of migraine headaches (severe, throbbing headaches that sometimes are accompanied by nausea or sensitivity to sound and light). Sumatriptan is in a class of medications called selective serotonin receptor agonists. It works by narrowing blood vessels in the head, stopping pain signals from being sent to the brain, and blocking the release of certain natural substances that cause pain, nausea, and other symptoms of migraine. Sumatriptan does not prevent migraine attacks or reduce the number of headaches you have.
Related Packages: 51407-0012-09Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Sumatriptan
Product Information
| NDC | 51407-0012 |
|---|---|
| Product ID | 51407-012_03881eee-d7cc-b0f0-e063-6394a90a5639 |
| Associated GPIs | 67406070100310 |
| GCN Sequence Number | 022479 |
| GCN Sequence Number Description | sumatriptan succinate TABLET 50 MG ORAL |
| HIC3 | H3F |
| HIC3 Description | ANTIMIGRAINE PREPARATIONS |
| GCN | 05700 |
| HICL Sequence Number | 006587 |
| HICL Sequence Number Description | SUMATRIPTAN SUCCINATE |
| Brand/Generic | Generic |
| Proprietary Name | Sumatriptan Succinate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | sumatriptan succinate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/1 |
| Substance Name | SUMATRIPTAN SUCCINATE |
| Labeler Name | Golden State Medical Supply, Inc. |
| Pharmaceutical Class | Serotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA077744 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 51407-0012-09 (51407001209)
| NDC Package Code | 51407-012-09 |
|---|---|
| Billing NDC | 51407001209 |
| Package | 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-012-09) |
| Marketing Start Date | 2018-02-12 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |