NDC 68151-0183 Losartan Potassium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-0183 - Losartan Potassium
Product Characteristics
Product Packages
NDC Code 68151-0183-9
Package Description: 1 TABLET, FILM COATED in 1 PACKAGE
Product Details
What is NDC 68151-0183?
What are the uses for Losartan Potassium?
Which are Losartan Potassium UNII Codes?
The UNII codes for the active ingredients in this product are:
- LOSARTAN POTASSIUM (UNII: 3ST302B24A)
- LOSARTAN (UNII: JMS50MPO89) (Active Moiety)
Which are Losartan Potassium 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:
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- INDIGOTINDISULFONATE SODIUM (UNII: D3741U8K7L)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Losartan Potassium?
- RxCUI: 979492 - losartan potassium 50 MG Oral Tablet
- RxCUI: 979492 - Losartan K+ 50 MG Oral Tablet
- RxCUI: 979492 - Losartan Pot 50 MG 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".