NDC 50090-3957 Omega-3-acid Ethyl Esters
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-3957 - Omega-3-acid Ethyl Esters
Product Characteristics
Product Packages
NDC Code 50090-3957-0
Package Description: 120 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 50090-3957?
What are the uses for Omega-3-acid Ethyl Esters?
Which are Omega-3-acid Ethyl Esters UNII Codes?
The UNII codes for the active ingredients in this product are:
- OMEGA-3-ACID ETHYL ESTERS (UNII: D87YGH4Z0Q)
- OMEGA-3 FATTY ACIDS (UNII: 71M78END5S) (Active Moiety)
Which are Omega-3-acid Ethyl Esters 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:
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- SHELLAC (UNII: 46N107B71O)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- AMMONIA (UNII: 5138Q19F1X)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Omega-3-acid Ethyl Esters?
- RxCUI: 577208 - omega-3 acid ethyl esters 1 GM Oral Capsule
- RxCUI: 577208 - omega-3 acid ethyl esters (USP) 1000 MG Oral Capsule
- RxCUI: 577208 - omega-3 acid ethyl esters 1 GM (at least 900 MG) Oral Capsule
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Patient Education
Omega-3 Fatty Acids
Omega-3 fatty acids are used together with lifestyle changes (diet, weight-loss, exercise) to reduce the amount of triglycerides (a fat-like substance) in the blood in people with very high triglycerides. Omega-3 fatty acids are in a class of medications called antilipemic or lipid-regulating agents. Omega-3 fatty acids may work by decreasing the amount of triglycerides and other fats made in the liver.
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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".