NDC 65044-4813 Animal Allergens, Ap Cattle Hair And Dander
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65044 - Jubilant Hollisterstier Llc
- 65044-4813 - Animal Allergens, Ap Cattle Hair And Dander
Product Packages
NDC Code 65044-4813-5
Package Description: 5 mL in 1 VIAL
Product Details
What is NDC 65044-4813?
What are the uses for Animal Allergens, Ap Cattle Hair And Dander?
Which are Animal Allergens, Ap Cattle Hair And Dander UNII Codes?
The UNII codes for the active ingredients in this product are:
- EQUUS CABALLUS HAIR (UNII: 4F35XG0149)
- EQUUS CABALLUS HAIR (UNII: 4F35XG0149) (Active Moiety)
- EQUUS CABALLUS DANDER (UNII: J81SZ18495)
- EQUUS CABALLUS DANDER (UNII: J81SZ18495) (Active Moiety)
- BOS TAURUS HAIR (UNII: TOQ97Z8644)
- BOS TAURUS HAIR (UNII: TOQ97Z8644) (Active Moiety)
- BOS TAURUS DANDER (UNII: C8VYS726O8)
- BOS TAURUS DANDER (UNII: C8VYS726O8) (Active Moiety)
Which are Animal Allergens, Ap Cattle Hair And Dander 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:
- PHENOL (UNII: 339NCG44TV)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Animal Allergens, Ap Cattle Hair And Dander?
- RxCUI: 1006369 - Canada goldenrod pollen extract 500 UNT/ML Injectable Solution
- RxCUI: 1006369 - Solidago canadensis pollen extract 500 UNT/ML Injectable Solution
- RxCUI: 1087970 - Mucor racemosus allergenic extract 1000 UNT/mL Injectable Solution
- RxCUI: 1087970 - Mucor racemosus allergenic extract 1000 UNT/ML Injectable Solution
- RxCUI: 1087970 - Mucor racemosus extract 1000 UNT/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".