NDC 66312-540 Citanest Forte
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66312 - Dentsply Pharmaceutical Inc.
- 66312-540 - Citanest Forte
Product Packages
NDC Code 66312-540-14
Package Description: 100 CARTRIDGE in 1 CARTON / 1.7 mL in 1 CARTRIDGE
NDC Code 66312-540-16
Package Description: 50 CARTRIDGE in 1 CARTON / 1.7 mL in 1 CARTRIDGE
Product Details
What is NDC 66312-540?
What are the uses for Citanest Forte?
Which are Citanest Forte UNII Codes?
The UNII codes for the active ingredients in this product are:
- PRILOCAINE HYDROCHLORIDE (UNII: MJW015BAPH)
- PRILOCAINE (UNII: 046O35D44R) (Active Moiety)
- EPINEPHRINE BITARTRATE (UNII: 30Q7KI53AK)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
Which are Citanest Forte 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Citanest Forte?
- RxCUI: 1012709 - Citanest Forte 4 % / 1:200,000 in 1.7 ML Cartridge
- RxCUI: 1012709 - 1.7 ML epinephrine 0.005 MG/ML / prilocaine hydrochloride 40 MG/ML Cartridge [Citanest Forte]
- RxCUI: 1012709 - Citanest Forte (prilocaine HCl 4 % / epineprine (as epinephrine bitartrate) 1:200,000) in 1.7 ML Cartridge
- RxCUI: 1595042 - prilocaine HCl 4 % / EPINEPHrine 1:200,000 in 1.7 ML Cartridge
- RxCUI: 1595042 - 1.7 ML epinephrine 0.005 MG/ML / prilocaine hydrochloride 40 MG/ML Cartridge
* Please review the disclaimer below.
[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".