NDC 54575-336 Apricot
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54575 - Allergy Laboratories, Inc.
- 54575-336 - Apricot
Product Packages
NDC Code 54575-336-02
Package Description: 2 mL in 1 VIAL, MULTI-DOSE
NDC Code 54575-336-10
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
NDC Code 54575-336-30
Package Description: 30 mL in 1 VIAL, MULTI-DOSE
NDC Code 54575-336-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 54575-336?
What are the uses for Apricot?
Which are Apricot UNII Codes?
The UNII codes for the active ingredients in this product are:
- APPLE (UNII: B423VGH5S9)
- APPLE (UNII: B423VGH5S9) (Active Moiety)
- APRICOT (UNII: 269CJD5GZ9)
- APRICOT (UNII: 269CJD5GZ9) (Active Moiety)
Which are Apricot 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Apricot?
- RxCUI: 1000013 - whole wheat allergenic extract 50 MG/ML Injectable Solution
- RxCUI: 1000013 - whole wheat allergenic extract 0.05 GM/ML Injectable Solution
- RxCUI: 1000013 - whole wheat extract 50 MG/ML Injectable Solution
- RxCUI: 1006300 - Aspergillus niger var. niger allergenic extract 50 MG/ML Injectable Solution
- RxCUI: 1006300 - Aspergillus niger var. niger allergenic extract 0.05 GM/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".