NDC 68151-0639 Lithium Carbonate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-0639 - Lithium Carbonate
Product Characteristics
Product Packages
NDC Code 68151-0639-2
Package Description: 1 TABLET, EXTENDED RELEASE in 1 PACKAGE
Product Details
What is NDC 68151-0639?
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:
- CALCIUM STEARATE (UNII: 776XM7047L)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SORBITOL (UNII: 506T60A25R)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Lithium Carbonate?
- RxCUI: 197891 - lithium carbonate 300 MG Extended Release Oral Tablet
- RxCUI: 197891 - LiCO3 300 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".