NDC 76519-1017 Sprix
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76519 - H.j. Harkins Company, Inc.
- 76519-1017 - Sprix
Product Packages
NDC Code 76519-1017-1
Package Description: 1 SPRAY, METERED in 1 BOTTLE, SPRAY
Product Details
What is NDC 76519-1017?
What are the uses for Sprix?
Which are Sprix UNII Codes?
The UNII codes for the active ingredients in this product are:
- KETOROLAC TROMETHAMINE (UNII: 4EVE5946BQ)
- KETOROLAC (UNII: YZI5105V0L) (Active Moiety)
Which are Sprix 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:
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POTASSIUM PHOSPHATE, MONOBASIC (UNII: 4J9FJ0HL51)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Sprix?
- RxCUI: 1797855 - ketorolac tromethamine 15.75 MG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1797855 - ketorolac tromethamine 15.8 MG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1797857 - SPRIX 15.75 MG/ACTUAT Metered Dose Nasal Spray
- RxCUI: 1797857 - ketorolac tromethamine 15.8 MG/ACTUAT Metered Dose Nasal Spray [Sprix]
- RxCUI: 1797857 - Sprix 15.75 MG/ACTUAT Metered Dose Nasal Spray
* 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".