NDC 66336-624 Kaletra
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 66336-624?
What are the uses for Kaletra?
Which are Kaletra UNII Codes?
The UNII codes for the active ingredients in this product are:
- LOPINAVIR (UNII: 2494G1JF75)
- LOPINAVIR (UNII: 2494G1JF75) (Active Moiety)
- RITONAVIR (UNII: O3J8G9O825)
- RITONAVIR (UNII: O3J8G9O825) (Active Moiety)
Which are Kaletra 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:
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- TALC (UNII: 7SEV7J4R1U)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- COPOVIDONE K25-31 (UNII: D9C330MD8B)
What is the NDC to RxNorm Crosswalk for Kaletra?
- RxCUI: 597730 - lopinavir 200 MG / ritonavir 50 MG Oral Tablet
- RxCUI: 847741 - Kaletra 200 MG / 50 MG Oral Tablet
- RxCUI: 847741 - lopinavir 200 MG / ritonavir 50 MG Oral Tablet [Kaletra]
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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".