NDC 61748-025 Ethosuximide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61748 - Akorn
- 61748-025 - Ethosuximide
Product Characteristics
Product Packages
Product Details
What is NDC 61748-025?
What are the uses for Ethosuximide?
Which are Ethosuximide UNII Codes?
The UNII codes for the active ingredients in this product are:
- ETHOSUXIMIDE (UNII: 5SEH9X1D1D)
- ETHOSUXIMIDE (UNII: 5SEH9X1D1D) (Active Moiety)
Which are Ethosuximide 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:
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- GELATIN (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Ethosuximide?
- RxCUI: 197682 - ethosuximide 250 MG Oral Capsule
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Patient Education
Ethosuximide
Ethosuximide is used to control absence seizures (petit mal) (a type of seizure in which there is a very short loss of awareness during which the person may stare straight ahead or blink his eyes and does not respond to others). Ethosuximide is in a class of medications called anticonvulsants. It works by reducing abnormal electrical activity in the brain.
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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".