NDC 51662-1589 Lidocaine Hcl And Epi
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51662 - Hf Acquisition Co Llc, Dba Healthfirst
- 51662-1589 - Lidocaine Hcl And Epi
Product Packages
NDC Code 51662-1589-3
Package Description: 25 POUCH in 1 CASE / 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1589-2) / 50 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 51662-1589?
What are the uses for Lidocaine Hcl And Epi?
Which are Lidocaine Hcl And Epi UNII Codes?
The UNII codes for the active ingredients in this product are:
- EPINEPHRINE BITARTRATE (UNII: 30Q7KI53AK)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- LIDOCAINE HYDROCHLORIDE ANHYDROUS (UNII: EC2CNF7XFP)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Lidocaine Hcl And Epi 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)
- BISULFITE ION (UNII: OJ9787WBLU)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for Lidocaine Hcl And Epi?
- RxCUI: 1010751 - lidocaine HCl 1 % / EPINEPHrine 1:100,000 Injectable Solution
- RxCUI: 1010751 - epinephrine 0.01 MG/ML / lidocaine hydrochloride 10 MG/ML Injectable Solution
- RxCUI: 1010751 - epinephrine (as epinephrine bitartrate) 1:100,000 / lidocaine hydrochloride 1 % Injectable Solution
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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".