NDC 70882-106 Atorvastatin Calcium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70882 - Cambridge Therapeutics Technologies, Llc
- 70882-106 - Atorvastatin Calcium
Product Characteristics
Product Packages
NDC Code 70882-106-30
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK
Price per Unit: $0.07347 per EA
Product Details
What is NDC 70882-106?
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 (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:
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- GLYCERIN (UNII: PDC6A3C0OX)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STARCH, CORN (UNII: O8232NY3SJ)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TALC (UNII: 7SEV7J4R1U)
- TROMETHAMINE (UNII: 023C2WHX2V)
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
- RxCUI: 617312 - atorvastatin calcium 10 MG Oral Tablet
- RxCUI: 617312 - atorvastatin 10 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".