NDC 68258-3008 Sumatriptan Succinate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68258 - Dispensing Solutions Inc.
- 68258-3008 - Sumatriptan Succinate
Product Characteristics
Product Packages
NDC Code 68258-3008-1
Package Description: 9 TABLET, FILM COATED in 1 BLISTER PACK
Product Details
What is NDC 68258-3008?
What are the uses for Sumatriptan Succinate?
Which are Sumatriptan Succinate 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 Succinate 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)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
What is the NDC to RxNorm Crosswalk for Sumatriptan Succinate?
- 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
- RxCUI: 313161 - SUMAtriptan succinate 50 MG Oral Tablet
- RxCUI: 313161 - sumatriptan 50 MG Oral Tablet
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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".