NDC 50090-3321 Xylocaine Mpf
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-3321 - Xylocaine
Product Packages
NDC Code 50090-3321-1
Package Description: 20 mL in 1 VIAL, SINGLE-DOSE
Product Details
What is NDC 50090-3321?
What are the uses for Xylocaine Mpf?
Which are Xylocaine Mpf UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE HYDROCHLORIDE ANHYDROUS (UNII: EC2CNF7XFP)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- EPINEPHRINE BITARTRATE (UNII: 30Q7KI53AK)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
Which are Xylocaine Mpf 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 CHLORIDE (UNII: 451W47IQ8X)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for Xylocaine Mpf?
- RxCUI: 1010688 - lidocaine HCl 2 % / EPINEPHrine 1:200,000 in 20 ML Injection
- RxCUI: 1010688 - 20 ML epinephrine 0.005 MG/ML / lidocaine hydrochloride 20 MG/ML Injection
- RxCUI: 1010688 - lidocaine HCl 2 % / EPINEPHrine 1:200,000 per 20 ML Injection
- RxCUI: 1010692 - Xylocaine 2 % / EPINEPHrine 1:200,000 in 20 ML Injection
- RxCUI: 1010692 - 20 ML epinephrine 0.005 MG/ML / lidocaine hydrochloride 20 MG/ML Injection [Xylocaine with Epinephrine]
* 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".