NDC 54868-5340 Lithium Carbonate
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Product Details
What is NDC 54868-5340?
What are the uses for Lithium Carbonate?
Which are Lithium Carbonate UNII Codes?
The UNII codes for the active ingredients in this product are:
- LITHIUM CARBONATE (UNII: 2BMD2GNA4V)
- LITHIUM CATION (UNII: 8H8Z5UER66) (Active Moiety)
Which are Lithium Carbonate 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:
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- STARCH, CORN (UNII: O8232NY3SJ)
- ALGINIC ACID (UNII: 8C3Z4148WZ)
What is the NDC to RxNorm Crosswalk for Lithium Carbonate?
- RxCUI: 197892 - lithium carbonate 450 MG Extended Release Oral Tablet
- RxCUI: 197892 - LiCO3 450 MG Extended Release 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".