NDC 16590-334 Prilosec
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Product Details
What is NDC 16590-334?
What are the uses for Prilosec?
Which are Prilosec UNII Codes?
The UNII codes for the active ingredients in this product are:
- OMEPRAZOLE MAGNESIUM (UNII: 426QFE7XLK)
- OMEPRAZOLE MAGNESIUM (UNII: 426QFE7XLK) (Active Moiety)
Which are Prilosec 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:
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
What is the NDC to RxNorm Crosswalk for Prilosec?
- RxCUI: 198051 - omeprazole 20 MG Delayed Release Oral Capsule
- RxCUI: 198051 - omeprazole 20 MG (as omeprazole magnesium 20.6 MG) Delayed Release Oral Capsule
- RxCUI: 207212 - PriLOSEC 20 MG Delayed Release Oral Capsule
- RxCUI: 207212 - omeprazole 20 MG Delayed Release Oral Capsule [Prilosec]
- RxCUI: 207212 - Prilosec 20 MG Delayed Release Oral Capsule
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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".