NDC 50090-2762 Ketorolac Tromethamine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-2762 - Ketorolac Tromethamine
Product Packages
NDC Code 50090-2762-0
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 5 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 50090-2762?
What are the uses for Ketorolac Tromethamine?
Which are Ketorolac Tromethamine UNII Codes?
The UNII codes for the active ingredients in this product are:
- KETOROLAC TROMETHAMINE (UNII: 4EVE5946BQ)
- KETOROLAC (UNII: YZI5105V0L) (Active Moiety)
Which are Ketorolac Tromethamine 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)
- OCTOXYNOL-40 (UNII: 9T1C662FKS)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for Ketorolac Tromethamine?
- RxCUI: 860107 - ketorolac tromethamine 0.5 % Ophthalmic Solution
- RxCUI: 860107 - ketorolac tromethamine 5 MG/ML Ophthalmic Solution
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Patient Education
Ketorolac Ophthalmic
Ophthalmic ketorolac is used to treat itchy eyes caused by allergies. It also is used to treat swelling and redness (inflammation) that can occur after cataract surgery. Ketorolac is in a class of medications called nonsteroidal anti-inflammatory drugs (NSAIDs). It works by stopping the release of substances that cause allergy symptoms and inflammation.
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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".