NDC 54868-5179 Caduet
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5179 - Caduet
Product Characteristics
10 MM
9 MM
11 MM
14 MM
PFIZER;CDT;254
PFIZER;CDT;051
PFIZER;CDT;052
PFIZER;CDT;054
Product Packages
NDC Code 54868-5179-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 54868-5179?
What are the uses for Caduet?
Which are Caduet UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMLODIPINE BESYLATE (UNII: 864V2Q084H)
- AMLODIPINE (UNII: 1J444QC288) (Active Moiety)
- ATORVASTATIN CALCIUM (UNII: 48A5M73Z4Q)
- ATORVASTATIN (UNII: A0JWA85V8F) (Active Moiety)
Which are Caduet 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:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- WATER (UNII: 059QF0KO0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 3000 (UNII: SA1B764746)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Caduet?
- RxCUI: 404011 - amLODIPine besylate 5 MG / atorvastatin calcium 80 MG Oral Tablet
- RxCUI: 404011 - amlodipine 5 MG / atorvastatin 80 MG Oral Tablet
- RxCUI: 404011 - amlodipine (as amlodipine besylate) 5 MG / atorvastatin (as atorvastatin calcium) 80 MG Oral Tablet
- RxCUI: 404013 - amLODIPine besylate 10 MG / atorvastatin calcium 80 MG Oral Tablet
- RxCUI: 404013 - amlodipine 10 MG / atorvastatin 80 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".