NDC 76135-005 Octreotide Acetate
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What is NDC 76135-005?
What are the uses for Octreotide Acetate?
Which are Octreotide Acetate UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTREOTIDE ACETATE (UNII: 75R0U2568I)
- OCTREOTIDE (UNII: RWM8CCW8GP) (Active Moiety)
Which are Octreotide Acetate 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:
- ACETIC ACID (UNII: Q40Q9N063P)
- SODIUM ACETATE (UNII: 4550K0SC9B)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- PHENOL (UNII: 339NCG44TV)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Octreotide Acetate?
- RxCUI: 312071 - octreotide 1000 MCG/ML Injectable Solution
- RxCUI: 312071 - octreotide 1 MG/ML Injectable Solution
- RxCUI: 312071 - octreotide (as octreotide acetate) 1000 MCG/ML Injectable Solution
- RxCUI: 314152 - octreotide 200 MCG/ML Injectable Solution
- RxCUI: 314152 - octreotide 0.2 MG/ML Injectable Solution
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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".