NDC 54868-5726 Metoprolol Tartrate
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What is NDC 54868-5726?
What are the uses for Metoprolol Tartrate?
Which are Metoprolol Tartrate UNII Codes?
The UNII codes for the active ingredients in this product are:
- METOPROLOL TARTRATE (UNII: W5S57Y3A5L)
- METOPROLOL (UNII: GEB06NHM23) (Active Moiety)
Which are Metoprolol Tartrate 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Metoprolol Tartrate?
- RxCUI: 866508 - metoprolol tartrate 5 MG in 5 ML Injection
- RxCUI: 866508 - 5 ML metoprolol tartrate 1 MG/ML Injection
- RxCUI: 866508 - metoprolol tartrate 5 MG per 5 ML Injection
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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".