NDC 50090-5569 Epinephrine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-5569 - Epinephrine
Product Packages
NDC Code 50090-5569-0
Package Description: 10 VIAL in 1 PACKAGE / 10 mL in 1 VIAL
Product Details
What is NDC 50090-5569?
What are the uses for Epinephrine?
Which are Epinephrine UNII Codes?
The UNII codes for the active ingredients in this product are:
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
Which are Epinephrine 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 BISULFITE (UNII: TZX5469Z6I)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
What is the NDC to RxNorm Crosswalk for Epinephrine?
- RxCUI: 727373 - EPINEPHrine 1 MG in 10 ML Prefilled Syringe
- RxCUI: 727373 - 10 ML epinephrine 0.1 MG/ML Prefilled Syringe
- RxCUI: 727373 - epinephrine 1 MG per 10 ML Prefilled Syringe
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Patient Education
Epinephrine Injection
Epinephrine injection is used along with emergency medical treatment to treat life-threatening allergic reactions caused by insect bites or stings, foods, medications, latex, and other causes. Epinephrine is in a class of medications called alpha- and beta-adrenergic agonists (sympathomimetic agents). It works by relaxing the muscles in the airways and tightening the blood vessels.
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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".