NDC 45865-726 Atorvastatin Calcium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 45865 - Medsource Pharmaceuticals
- 45865-726 - Atorvastatin Calcium
Product Characteristics
Product Packages
NDC Code 45865-726-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
NDC Code 45865-726-49
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 45865-726?
What are the uses for Atorvastatin Calcium?
Which are Atorvastatin Calcium UNII Codes?
The UNII codes for the active ingredients in this product are:
- ATORVASTATIN CALCIUM TRIHYDRATE (UNII: 48A5M73Z4Q)
- ATORVASTATIN (UNII: A0JWA85V8F) (Active Moiety)
Which are Atorvastatin Calcium 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:
- DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER (UNII: 905HNO1SIH)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYVINYL ALCOHOL (94000 MW) (UNII: C1MS7RRZ6L)
What is the NDC to RxNorm Crosswalk for Atorvastatin Calcium?
- RxCUI: 617310 - atorvastatin calcium 20 MG Oral Tablet
- RxCUI: 617310 - atorvastatin 20 MG Oral Tablet
- RxCUI: 617310 - atorvastatin (as atorvastatin calcium) 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".