NDC 62250-103 Epinephrine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62250 - Belcher Pharmaceuticals, Llc
- 62250-103 - Epinephrine
Product Packages
NDC Code 62250-103-10
Package Description: 10 AMPULE in 1 BOX / 1 mL in 1 AMPULE
Product Details
What is NDC 62250-103?
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 CHLORIDE (UNII: 451W47IQ8X)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Epinephrine?
- RxCUI: 1660014 - EPINEPHrine 1 MG in 1 ML Injection
- RxCUI: 1660014 - 1 ML epinephrine 1 MG/ML Injection
- RxCUI: 1660014 - epinephrine 1 MG per 1 ML Injection
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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".