NDC 54868-5034 Antabuse
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Product Information
Product Characteristics
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Product Details
What is NDC 54868-5034?
What are the uses for Antabuse?
Which are Antabuse UNII Codes?
The UNII codes for the active ingredients in this product are:
- DISULFIRAM (UNII: TR3MLJ1UAI)
- DISULFIRAM (UNII: TR3MLJ1UAI) (Active Moiety)
Which are Antabuse 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Antabuse?
- RxCUI: 197623 - disulfiram 250 MG Oral Tablet
- RxCUI: 210628 - Antabuse 250 MG Oral Tablet
- RxCUI: 210628 - disulfiram 250 MG Oral Tablet [Antabuse]
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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".