NDC 63776-385 Osteosis
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63776-385?
What are the uses for Osteosis?
Which are Osteosis UNII Codes?
The UNII codes for the active ingredients in this product are:
- BOS TAURUS BONE (UNII: TRS31EO6ZN)
- BOS TAURUS BONE (UNII: TRS31EO6ZN) (Active Moiety)
- SUS SCROFA BONE (UNII: 597RLJ09RG)
- SUS SCROFA BONE (UNII: 597RLJ09RG) (Active Moiety)
- CALCITONIN (UNII: DF35I47HCM)
- CALCITONIN (UNII: DF35I47HCM) (Active Moiety)
- BOS TAURUS CARTILAGE (UNII: UE77B10IIY)
- BOS TAURUS CARTILAGE (UNII: UE77B10IIY) (Active Moiety)
- SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F)
- SUS SCROFA CARTILAGE (UNII: 73ECW5WG2F) (Active Moiety)
- BOS TAURUS RED BLOOD CELL (UNII: 5W4FLB0U2C)
- BOS TAURUS RED BLOOD CELL (UNII: 5W4FLB0U2C) (Active Moiety)
- SUS SCROFA RED BLOOD CELL (UNII: 5X23IGF970)
- SUS SCROFA RED BLOOD CELL (UNII: 5X23IGF970) (Active Moiety)
- INTERLEUKIN-3 (UNII: A802907MI4)
- INTERLEUKIN-3 (UNII: A802907MI4) (Active Moiety)
- BOS TAURUS PARATHYROID GLAND (UNII: SMV71DDI4T)
- BOS TAURUS PARATHYROID GLAND (UNII: SMV71DDI4T) (Active Moiety)
- SUS SCROFA PARATHYROID GLAND (UNII: 2KBE35NE8S)
- SUS SCROFA PARATHYROID GLAND (UNII: 2KBE35NE8S) (Active Moiety)
- VITAMIN D (UNII: 9VU1KI44GP)
- VITAMIN D (UNII: 9VU1KI44GP) (Active Moiety)
Which are Osteosis 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* 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".