NDC 53808-0766 Pravastatin Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-0766 - Pravastatin Sodium
Product Characteristics
YELLOW (C48330 - LIGHT YELLOW)
8 MM
93;7201
Product Packages
NDC Code 53808-0766-1
Package Description: 30 TABLET in 1 BLISTER PACK
Product Details
What is NDC 53808-0766?
What are the uses for Pravastatin Sodium?
Which are Pravastatin Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- PRAVASTATIN SODIUM (UNII: 3M8608UQ61)
- PRAVASTATIN (UNII: KXO2KT9N0G) (Active Moiety)
Which are Pravastatin Sodium 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:
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- CROSPOVIDONE (UNII: 68401960MK)
- LACTOSE (UNII: J2B2A4N98G)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Pravastatin Sodium?
- RxCUI: 904458 - pravastatin sodium 10 MG Oral Tablet
- RxCUI: 904467 - pravastatin sodium 20 MG Oral Tablet
- RxCUI: 904475 - pravastatin sodium 40 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".