NDC 65044-0547 Standardized Grass Pollen, Bluegrass, Kentucky June
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65044 - Jubilant Hollisterstier Llc
- 65044-0547 - Standardized Grass Pollen, Bluegrass, Kentucky June
Product Packages
NDC Code 65044-0547-5
Package Description: 5 mL in 1 VIAL
Product Details
What is NDC 65044-0547?
What are the uses for Standardized Grass Pollen, Bluegrass, Kentucky June?
Which are Standardized Grass Pollen, Bluegrass, Kentucky June UNII Codes?
The UNII codes for the active ingredients in this product are:
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T)
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (Active Moiety)
Which are Standardized Grass Pollen, Bluegrass, Kentucky June 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)
- PHENOL (UNII: 339NCG44TV)
- ALBUMIN HUMAN (UNII: ZIF514RVZR)
What is the NDC to RxNorm Crosswalk for Standardized Grass Pollen, Bluegrass, Kentucky June?
- RxCUI: 853988 - Bermuda grass pollen extract 100 BAU/ML Injectable Solution
- RxCUI: 853988 - Cynodon dactylon pollen extract 100 BAU/ML Injectable Solution
- RxCUI: 853990 - orchard grass pollen extract 100 BAU/ML Injectable Solution
- RxCUI: 853990 - Dactylis glomerata pollen extract 100 BAU/ML Injectable Solution
- RxCUI: 853992 - orchard grass pollen extract 1000 BAU/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".