NDC 53217-169 Fenoprofen Calcium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53217 - Aidarex Pharmaceuticals Llc
- 53217-169 - Fenoprofen Calcium
Product Characteristics
BLUE (C48333 - OPAQUE BLUE)
Product Packages
NDC Code 53217-169-90
Package Description: 90 CAPSULE in 1 BOTTLE
Product Details
What is NDC 53217-169?
What are the uses for Fenoprofen Calcium?
Which are Fenoprofen Calcium UNII Codes?
The UNII codes for the active ingredients in this product are:
- FENOPROFEN CALCIUM (UNII: 0X2CW1QABJ)
- FENOPROFEN (UNII: RA33EAC7KY) (Active Moiety)
Which are Fenoprofen Calcium 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)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TALC (UNII: 7SEV7J4R1U)
- GELATIN (UNII: 2G86QN327L)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Fenoprofen Calcium?
- RxCUI: 858116 - fenoprofen calcium 400 MG Oral Capsule
- RxCUI: 858116 - fenoprofen 400 MG Oral Capsule
- RxCUI: 858116 - fenoprofen (as fenoprofen calcium) 400 MG Oral Capsule
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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".