NDC 12634-809 Ketorolac Tromethamine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 12634-809-00
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 12634-809-01
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 12634-809-25
Package Description: 25 TABLET in 1 BLISTER PACK
NDC Code 12634-809-55
Package Description: 15 TABLET in 1 BLISTER PACK
NDC Code 12634-809-57
Package Description: 20 TABLET in 1 BLISTER PACK
NDC Code 12634-809-59
Package Description: 30 TABLET in 1 BLISTER PACK
NDC Code 12634-809-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 12634-809-61
Package Description: 10 TABLET in 1 BLISTER PACK
NDC Code 12634-809-65
Package Description: 5 TABLET in 1 BLISTER PACK
NDC Code 12634-809-66
Package Description: 6 TABLET in 1 BLISTER PACK
NDC Code 12634-809-71
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 12634-809-79
Package Description: 25 TABLET in 1 BOTTLE
NDC Code 12634-809-80
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 12634-809-85
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 12634-809-91
Package Description: 1 TABLET in 1 BLISTER PACK
NDC Code 12634-809-95
Package Description: 5 TABLET in 1 BOTTLE
NDC Code 12634-809-96
Package Description: 6 TABLET in 1 BOTTLE
Product Details
What is NDC 12634-809?
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:
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Ketorolac Tromethamine?
- RxCUI: 834022 - ketorolac tromethamine 10 MG Oral Tablet
* 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".