NDC 17856-3120 Calcitriol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corp.
- 17856-3120 - Calcitriol
Product Packages
NDC Code 17856-3120-1
Package Description: 120 SYRINGE in 1 BOX, UNIT-DOSE / .5 mL in 1 SYRINGE
Product Details
What is NDC 17856-3120?
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:
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- OMEGA-3-ACID ETHYL ESTERS (UNII: D87YGH4Z0Q)
What is the NDC to RxNorm Crosswalk for Calcitriol?
- RxCUI: 313932 - calcitriol 1 MCG in 1 mL Oral Solution
- RxCUI: 313932 - calcitriol 0.001 MG/ML Oral Solution
- RxCUI: 313932 - calcitriol 1 MCG per 1 ML Oral Solution
* Please review the disclaimer below.
Patient Education
Calcitriol
Calcitriol is used to treat and prevent low levels of calcium and bone disease in patients whose kidneys or parathyroid glands (glands in the neck that release natural substances to control the amount of calcium in the blood) are not working normally. It is also used to treat secondary hyperparathyroidism (a condition in which the body produces too much parathyroid hormone [PTH; a natural substance needed to control the amount of calcium in the blood]) and metabolic bone disease in people with kidney disease. Calcitriol is in a class of medications called vitamin D analogs. It works by helping the body to use more of the calcium found in foods or supplements and regulating the body's production of parathyroid hormone.
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* Please review the disclaimer below.
[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".