NDC 53217-278 Fosinopril Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
10 MM
IG;202
Code Structure Chart
Product Details
What is NDC 53217-278?
What are the uses for Fosinopril Sodium?
Which are Fosinopril Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- FOSINOPRIL SODIUM (UNII: NW2RTH6T2N)
- FOSINOPRILAT (UNII: S312EY6ZT8) (Active Moiety)
Which are Fosinopril Sodium 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)
- LACTOSE (UNII: J2B2A4N98G)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
What is the NDC to RxNorm Crosswalk for Fosinopril Sodium?
- RxCUI: 857169 - fosinopril sodium 10 MG Oral Tablet
- RxCUI: 857169 - FNP Sodium 10 MG Oral Tablet
- RxCUI: 857187 - fosinopril sodium 40 MG Oral Tablet
- RxCUI: 857187 - FNP Sodium 40 MG Oral Tablet
* Please review the disclaimer below.
[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".