NDC 68071-5072 Sumatriptan
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Product Details
What is NDC 68071-5072?
What are the uses for Sumatriptan?
Which are Sumatriptan UNII Codes?
The UNII codes for the active ingredients in this product are:
- SUMATRIPTAN SUCCINATE (UNII: J8BDZ68989)
- SUMATRIPTAN (UNII: 8R78F6L9VO) (Active Moiety)
Which are Sumatriptan Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
What is the NDC to RxNorm Crosswalk for Sumatriptan?
- RxCUI: 313160 - SUMAtriptan succinate 100 MG Oral Tablet
- RxCUI: 313160 - sumatriptan 100 MG Oral Tablet
- RxCUI: 313160 - sumatriptan 100 MG (as sumatriptan succinate 140 MG) Oral Tablet
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Patient Education
Sumatriptan
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.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".