NDC 76519-1017 Sprix

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
76519-1017
Proprietary Name:
Sprix
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
H.j. Harkins Company, Inc.
Labeler Code:
76519
Start Marketing Date: [9]
04-26-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76519-1017-1

Package Description: 1 SPRAY, METERED in 1 BOTTLE, SPRAY

Product Details

What is NDC 76519-1017?

The NDC code 76519-1017 is assigned by the FDA to the product Sprix which is product labeled by H.j. Harkins Company, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76519-1017-1 1 spray, metered in 1 bottle, spray . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Sprix?

Ketorolac is used for the short-term treatment (up to 5 days) of moderate to severe pain in adults, such as after surgery. Reducing pain helps you recover more comfortably so you can return to your normal daily activities. This medication is a nonsteroidal anti-inflammatory drug (NSAID). It works by decreasing inflammation, swelling, and pain.

Which are Sprix UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Sprix?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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

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Product Footnotes

[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".