NDC 53217-371 Etodolac
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53217 - Aidarex Pharmaceuticals Llc
- 53217-371 - Etodolac
Product Characteristics
Product Packages
NDC Code 53217-371-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE
NDC Code 53217-371-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
NDC Code 53217-371-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE
NDC Code 53217-371-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 53217-371?
What are the uses for Etodolac?
Which are Etodolac UNII Codes?
The UNII codes for the active ingredients in this product are:
- ETODOLAC (UNII: 2M36281008)
- ETODOLAC (UNII: 2M36281008) (Active Moiety)
Which are Etodolac 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:
- CROSPOVIDONE (UNII: 2S7830E561)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- HYPROMELLOSE 2208 (100 MPA.S) (UNII: B1QE5P712K)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHYLCELLULOSE (100 CPS) (UNII: 4GFU244C4J)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Etodolac?
- RxCUI: 197686 - etodolac 400 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".