NDC 50090-4555 Lidocaine Hydrochloride And Dextrose
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What is NDC 50090-4555?
What are the uses for Lidocaine Hydrochloride And Dextrose?
Which are Lidocaine Hydrochloride And Dextrose UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE ANHYDROUS (UNII: EC2CNF7XFP)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- DEXTROSE MONOHYDRATE (UNII: LX22YL083G)
- ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK) (Active Moiety)
Which are Lidocaine Hydrochloride And Dextrose 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:
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Lidocaine Hydrochloride And Dextrose?
- RxCUI: 1737723 - lidocaine HCl 0.8 % in 250 ML Injection
- RxCUI: 1737723 - 250 ML lidocaine hydrochloride 8 MG/ML Injection
- RxCUI: 1737723 - lidocaine HCl 0.8 % per 250 ML Injection
- RxCUI: 1737723 - lidocaine HCl 2 GM per 250 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".