NDC 69097-185 Pravastatin Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69097 - Cipla Usa Inc.
- 69097-185 - Pravastatin Sodium
Product Characteristics
11 MM
15 MM
C184
C185
Product Packages
NDC Code 69097-185-05
Package Description: 90 TABLET in 1 BOTTLE
NDC Code 69097-185-12
Package Description: 500 TABLET in 1 BOTTLE
NDC Code 69097-185-15
Package Description: 1000 TABLET in 1 BOTTLE
Product Details
What is NDC 69097-185?
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:
- MANNITOL (UNII: 3OWL53L36A)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED (UNII: 2165RE0K14)
- CROSPOVIDONE (UNII: 68401960MK)
- CALCIUM STEARATE (UNII: 776XM7047L)
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
- RxCUI: 904481 - pravastatin sodium 80 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".