NDC 54868-3726 Cozaar
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-3726 - Cozaar
Product Characteristics
10 MM
952
2
Product Packages
NDC Code 54868-3726-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
NDC Code 54868-3726-1
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-3726?
What are the uses for Cozaar?
Which are Cozaar UNII Codes?
The UNII codes for the active ingredients in this product are:
- LOSARTAN POTASSIUM (UNII: 3ST302B24A)
- LOSARTAN (UNII: JMS50MPO89) (Active Moiety)
Which are Cozaar 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- STARCH, CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
What is the NDC to RxNorm Crosswalk for Cozaar?
- RxCUI: 979480 - losartan potassium 100 MG Oral Tablet
- RxCUI: 979480 - Losartan K+ 100 MG Oral Tablet
- RxCUI: 979480 - Losartan Pot 100 MG Oral Tablet
- RxCUI: 979482 - Cozaar 100 MG Oral Tablet
- RxCUI: 979482 - losartan potassium 100 MG Oral Tablet [Cozaar]
* 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".