NDC 59746-433 Zolmitriptan
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
9 MM
CB8
1
Code Structure Chart
Product Details
What is NDC 59746-433?
What are the uses for Zolmitriptan?
Which are Zolmitriptan UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZOLMITRIPTAN (UNII: 2FS66TH3YW)
- ZOLMITRIPTAN (UNII: 2FS66TH3YW) (Active Moiety)
Which are Zolmitriptan 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
What is the NDC to RxNorm Crosswalk for Zolmitriptan?
- RxCUI: 200193 - ZOLMitriptan 2.5 MG Oral Tablet
- RxCUI: 200193 - zolmitriptan 2.5 MG Oral Tablet
- RxCUI: 200194 - ZOLMitriptan 5 MG Oral Tablet
- RxCUI: 200194 - zolmitriptan 5 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Zolmitriptan
Zolmitriptan is used to treat the symptoms of migraine headaches (severe throbbing headaches that sometimes are accompanied by nausea and sensitivity to sound and light). Zolmitriptan is in a class of medications called selective serotonin receptor agonists. It works by narrowing blood vessels around the brain, 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. Zolmitriptan does not prevent migraine attacks or reduce the number of headaches you have.
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* Please review the disclaimer below.
[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".