NDC 31382-557 Marcaine
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Product Details
What is NDC 31382-557?
What are the uses for Marcaine?
Which are Marcaine UNII Codes?
The UNII codes for the active ingredients in this product are:
- BUPIVACAINE HYDROCHLORIDE ANHYDROUS (UNII: AKA908P8J1)
- BUPIVACAINE (UNII: Y8335394RO) (Active Moiety)
- EPINEPHRINE BITARTRATE (UNII: 30Q7KI53AK)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
Which are Marcaine 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 METABISULFITE (UNII: 4VON5FNS3C)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- MONOTHIOGLYCEROL (UNII: AAO1P0WSXJ)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- EDETATE CALCIUM DISODIUM (UNII: 25IH6R4SGF)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Marcaine?
- RxCUI: 1670365 - BUPivacaine HCl 0.5 % / EPINEPHrine 1:200,000 in 1.8 ML Dental Cartridge
- RxCUI: 1670365 - 1.8 ML bupivacaine hydrochloride 5 MG/ML / epinephrine 0.005 MG/ML Cartridge
- RxCUI: 1670365 - bupivacaine HCl 0.5 % / epinephrine 1:200,000 per 1.8 ML Dental Cartridge
- RxCUI: 1673142 - Marcaine 0.5 % / EPINEPHrine 1:200,000 in 1.8 ML Dental Cartridge
- RxCUI: 1673142 - 1.8 ML bupivacaine hydrochloride 5 MG/ML / epinephrine 0.005 MG/ML Cartridge [Marcaine with Epinephrine]
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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".