NDC 53808-0650 Isentress
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 53808-0650?
What are the uses for Isentress?
Which are Isentress UNII Codes?
The UNII codes for the active ingredients in this product are:
- RALTEGRAVIR POTASSIUM (UNII: 43Y000U234)
- RALTEGRAVIR (UNII: 22VKV8053U) (Active Moiety)
Which are Isentress 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:
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Isentress?
- RxCUI: 744842 - raltegravir 400 MG Oral Tablet
- RxCUI: 744842 - raltegravir 400 MG (as raltegravir potassium 434.4 MG) Oral Tablet
- RxCUI: 744846 - Isentress 400 MG Oral Tablet
- RxCUI: 744846 - raltegravir 400 MG Oral Tablet [Isentress]
- RxCUI: 744846 - ISENTRESS 400 MG (as raltegravir potassium 434.4 MG) Oral Tablet
* Please review the disclaimer below.
[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".