NDC 54868-6036 Azor
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6036 - Azor
Product Characteristics
Product Packages
NDC Code 54868-6036-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-6036?
What are the uses for Azor?
Which are Azor UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMLODIPINE BESYLATE (UNII: 864V2Q084H)
- AMLODIPINE (UNII: 1J444QC288) (Active Moiety)
- OLMESARTAN MEDOXOMIL (UNII: 6M97XTV3HD)
- OLMESARTAN (UNII: 8W1IQP3U10) (Active Moiety)
Which are Azor 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)
- STARCH, CORN (UNII: O8232NY3SJ)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Azor?
- RxCUI: 730866 - amLODIPine 10 MG / olmesartan medoxomil 40 MG Oral Tablet
- RxCUI: 730866 - amlodipine 10 MG / olmesartan medoxomil 40 MG Oral Tablet
- RxCUI: 730866 - amlodipine 10 MG (as amlodipine besylate 13.9 MG) / olmesartan medoxomil 40 MG Oral Tablet
- RxCUI: 730869 - amLODIPine 5 MG / olmesartan medoxomil 20 MG Oral Tablet
- RxCUI: 730869 - amlodipine 5 MG / olmesartan medoxomil 20 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".