NDC 54868-6322 Atorvastatin Calcium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
12 MM
15 MM
19 MM
RX828
RX829
RX830
Code Structure Chart
Product Details
What is NDC 54868-6322?
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:
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CANDELILLA WAX (UNII: WL0328HX19)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- WATER (UNII: 059QF0KO0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- METHYLCELLULOSE (400 CPS) (UNII: O0GN6F9B2Y)
- POLYSORBATE 65 (UNII: 14BGY2Y3MJ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
What is the NDC to RxNorm Crosswalk for Atorvastatin Calcium?
- RxCUI: 259255 - atorvastatin calcium 80 MG Oral Tablet
- RxCUI: 259255 - atorvastatin 80 MG Oral Tablet
- RxCUI: 259255 - atorvastatin (as atorvastatin calcium) 80 MG Oral Tablet
- RxCUI: 617310 - atorvastatin calcium 20 MG Oral Tablet
- RxCUI: 617310 - atorvastatin 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".