NDC 69238-1606 Dihydroergotamine Mesylate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69238 - Amneal Pharmaceuticals Ny Llc
- 69238-1606 - Dihydroergotamine Mesylate
Product Packages
NDC Code 69238-1606-8
Package Description: 8 VIAL in 1 CARTON / 1 mL in 1 VIAL (69238-1606-1)
Price per Unit: $34.21179 per ML
Product Details
What is NDC 69238-1606?
What are the uses for Dihydroergotamine Mesylate?
Which are Dihydroergotamine Mesylate UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIHYDROERGOTAMINE MESYLATE (UNII: 81AXN7R2QT)
- DIHYDROERGOTAMINE (UNII: 436O5HM03C) (Active Moiety)
Which are Dihydroergotamine Mesylate 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:
- CAFFEINE (UNII: 3G6A5W338E)
- ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
- CARBON DIOXIDE (UNII: 142M471B3J)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Dihydroergotamine Mesylate?
- RxCUI: 861668 - dihydroergotamine mesylate 4 MG/mL Metered Dose Nasal Spray
- RxCUI: 861668 - dihydroergotamine mesylate 0.5 MG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 861668 - DHE Mesylate 0.5 MG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 861668 - dihydroergotamine mesylate 0.5 MG/ACTUAT (4 MG/ML) Metered Dose Nasal Spray
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Patient Education
Dihydroergotamine Nasal Spray
Dihydroergotamine is used to treat migraine headaches (severe, throbbing headaches that sometimes are accompanied by nausea and sensitivity to sound and light). Dihydroergotamine is in a class of medications called ergot alkaloids. It works by tightening blood vessels in the brain and by stopping the release of natural substances in the brain that cause swelling.
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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".