NDC 65044-3519 Food - Plant Source, Potato, White Solanum Tuberosum
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What is NDC 65044-3519?
What are the uses for Food - Plant Source, Potato, White Solanum Tuberosum?
Which are Food - Plant Source, Potato, White Solanum Tuberosum UNII Codes?
The UNII codes for the active ingredients in this product are:
- HAZELNUT, UNSPECIFIED (UNII: IW0OM96F6O)
- HAZELNUT, UNSPECIFIED (UNII: IW0OM96F6O) (Active Moiety)
- CANTALOUPE (UNII: 8QF5D5H6UH)
- CANTALOUPE (UNII: 8QF5D5H6UH) (Active Moiety)
- ORANGE (UNII: 5EVU04N5QU)
- ORANGE (UNII: 5EVU04N5QU) (Active Moiety)
- PEA (UNII: W4X7H8GYFM)
- PEA (UNII: W4X7H8GYFM) (Active Moiety)
- PEACH (UNII: 3OKE88I3QG)
- PEACH (UNII: 3OKE88I3QG) (Active Moiety)
- PEANUT (UNII: QE1QX6B99R)
- PEANUT (UNII: QE1QX6B99R) (Active Moiety)
- PECAN (UNII: F14P91GB5F)
- PECAN (UNII: F14P91GB5F) (Active Moiety)
- POTATO (UNII: CFE1S8DYWD)
- POTATO (UNII: CFE1S8DYWD) (Active Moiety)
Which are Food - Plant Source, Potato, White Solanum Tuberosum 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
What is the NDC to RxNorm Crosswalk for Food - Plant Source, Potato, White Solanum Tuberosum?
- RxCUI: 891663 - peanut allergenic extract 100 MG/ML Injectable Solution
- RxCUI: 891663 - peanut allergenic extract 0.1 GM/ML Injectable Solution
- RxCUI: 891675 - soybean allergenic extract 100 MG/ML Injectable Solution
- RxCUI: 891675 - soybean allergenic extract 0.1 GM/ML Injectable Solution
- RxCUI: 891681 - string bean allergenic extract 100 MG/ML Injectable Solution
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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".