NDC 49288-0656 Treatment Set Ts329678
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49288 - Antigen Laboratories, Inc.
- 49288-0656 - Treatment Set Ts329678
Product Packages
NDC Code 49288-0656-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 49288-0656?
What are the uses for Treatment Set Ts329678?
Which are Treatment Set Ts329678 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3)
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (Active Moiety)
- CYNODON DACTYLON POLLEN (UNII: 175F461W10)
- CYNODON DACTYLON POLLEN (UNII: 175F461W10) (Active Moiety)
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T)
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (Active Moiety)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (Active Moiety)
- QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK)
- QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (Active Moiety)
- CARYA ALBA POLLEN (UNII: G2A764T54B)
- CARYA ALBA POLLEN (UNII: G2A764T54B) (Active Moiety)
Which are Treatment Set Ts329678 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:
- WATER (UNII: 059QF0KO0R)
- PHENOL (UNII: 339NCG44TV)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Treatment Set Ts329678?
- RxCUI: 1191210 - dog hair extract 50 MG/ML / short ragweed pollen extract 800 AU/ML Injectable Solution
- RxCUI: 1191210 - Ambrosia artemisiifolia pollen extract 800 AU/ML / Canis lupus familiaris hair extract 50 MG/ML Injectable Solution
- RxCUI: 1192780 - American house dust mite allergenic extract 400 AU/mL / European house dust mite allergenic extract 2000 AU/mL Injectable Solution
- RxCUI: 1192780 - American house dust mite allergenic extract 400 AU/ML / European house dust mite allergenic extract 2000 AU/ML Injectable Solution
- RxCUI: 1192780 - American house dust mite extract 400 AU/ML / European house dust mite extract 2000 AU/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".