NDC 17856-0016 Phenobarbital
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 17856-0016?
What are the uses for Phenobarbital?
Which are Phenobarbital UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENOBARBITAL (UNII: YQE403BP4D)
- PHENOBARBITAL (UNII: YQE403BP4D) (Active Moiety)
Which are Phenobarbital 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:
- ALCOHOL (UNII: 3K9958V90M)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUCROSE (UNII: C151H8M554)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Phenobarbital?
- RxCUI: 702519 - PHENobarbital 20 MG in 5 mL Oral Solution
- RxCUI: 702519 - phenobarbital 4 MG/ML Oral Solution
- RxCUI: 702519 - phenobarbital 20 MG per 5 ML Oral Solution
- RxCUI: 702519 - phenobarbital 30 MG per 7.5 ML Oral Solution
- RxCUI: 702519 - phenobarbital 60 MG per 15 ML Oral 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".