NDC 17478-932 Calcitriol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17478 - Akorn
- 17478-932 - Calcitriol
Product Packages
NDC Code 17478-932-01
Package Description: 10 AMPULE in 1 CARTON / 1 mL in 1 AMPULE
Product Details
What is NDC 17478-932?
What are the uses for Calcitriol?
Which are Calcitriol UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALCITRIOL (UNII: FXC9231JVH)
- CALCITRIOL (UNII: FXC9231JVH) (Active Moiety)
Which are Calcitriol 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 PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM ASCORBATE (UNII: S033EH8359)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Calcitriol?
- RxCUI: 308869 - calcitriol 1 MCG in 1 ML Injection
- RxCUI: 308869 - 1 ML calcitriol 0.001 MG/ML Injection
- RxCUI: 308869 - calcitriol 1 MCG per 1 ML Injection
- RxCUI: 308870 - calcitriol 2 MCG in 1 ML Injection
- RxCUI: 308870 - 1 ML calcitriol 0.002 MG/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".