NDC 50090-4524 Atropine Sulfate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-4524 - Atropine Sulfate
Product Packages
NDC Code 50090-4524-0
Package Description: 1 mL in 1 VIAL, SINGLE-DOSE
Product Details
What is NDC 50090-4524?
What are the uses for Atropine Sulfate?
Which are Atropine Sulfate UNII Codes?
The UNII codes for the active ingredients in this product are:
- ATROPINE SULFATE (UNII: 03J5ZE7KA5)
- ATROPINE (UNII: 7C0697DR9I) (Active Moiety)
Which are Atropine Sulfate 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)
- SULFURIC ACID (UNII: O40UQP6WCF)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Atropine Sulfate?
- RxCUI: 1190795 - atropine sulfate 1 MG in 1 ML Injection
- RxCUI: 1190795 - 1 ML atropine sulfate 1 MG/ML Injection
- RxCUI: 1190795 - atropine sulfate 1 MG per 1 ML Injection
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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".