NDC 67296-1818 Tivicay
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 67296-1818?
What are the uses for Tivicay?
Which are Tivicay UNII Codes?
The UNII codes for the active ingredients in this product are:
- DOLUTEGRAVIR SODIUM (UNII: 1Q1V9V5WYQ)
- DOLUTEGRAVIR (UNII: DKO1W9H7M1) (Active Moiety)
Which are Tivicay 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:
- MANNITOL (UNII: 3OWL53L36A)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Tivicay?
- RxCUI: 1433873 - dolutegravir 50 MG Oral Tablet
- RxCUI: 1433873 - dolutegravir 50 MG (as dolutegravir sodium 52.6 MG) Oral Tablet
- RxCUI: 1433879 - Tivicay 50 MG Oral Tablet
- RxCUI: 1433879 - dolutegravir 50 MG Oral Tablet [Tivicay]
- RxCUI: 1433879 - Tivicay 50 MG (as dolutegravir sodium) Oral Tablet
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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".