NDC 65044-0614 Standardized Grass Pollen, Fescue, Meadow
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 65044-0614?
What are the uses for Standardized Grass Pollen, Fescue, Meadow?
Which are Standardized Grass Pollen, Fescue, Meadow 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)
- FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1)
- FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1) (Active Moiety)
Which are Standardized Grass Pollen, Fescue, Meadow 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, Fescue, Meadow?
- 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".