NDC 15631-0455 Veratrum Album
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 15631-0455-0
Package Description: 100 PELLET in 1 VIAL, SINGLE-DOSE
NDC Code 15631-0455-1
Package Description: 200 PELLET in 1 PACKAGE
NDC Code 15631-0455-2
Package Description: 400 PELLET in 1 PACKAGE
NDC Code 15631-0455-3
Package Description: 750 PELLET in 1 PACKAGE
NDC Code 15631-0455-4
Package Description: 2500 PELLET in 1 PACKAGE
NDC Code 15631-0455-5
Package Description: 12500 PELLET in 1 PACKAGE
Product Details
What is NDC 15631-0455?
What are the uses for Veratrum Album?
Which are Veratrum Album UNII Codes?
The UNII codes for the active ingredients in this product are:
- VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z)
- VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (Active Moiety)
Which are Veratrum Album 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:
- SUCROSE (UNII: C151H8M554)
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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".