Ketorolac Tromethamine
Ketorolac Tromethamine Injection, USP
Approved
Approval ID
6dd21587-12ce-4f43-9761-43bc73d96906
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 9, 2018
Manufacturers
FDA
A-S Medication Solutions
DUNS: 830016429
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
ketorolac tromethamine
PRODUCT DETAILS
NDC Product Code50090-3397
Application NumberANDA204216
Marketing CategoryC73584
Route of AdministrationINTRAMUSCULAR
Effective DateJanuary 15, 2017
Generic Nameketorolac tromethamine
INGREDIENTS (6)
KETOROLAC TROMETHAMINEActive
Quantity: 30 mg in 1 mL
Code: 4EVE5946BQ
Classification: ACTIB
sodium chlorideInactive
Code: 451W47IQ8X
Classification: IACT
sodium hydroxideInactive
Code: 55X04QC32I
Classification: IACT
alcoholInactive
Code: 3K9958V90M
Classification: IACT
hydrochloric acidInactive
Code: QTT17582CB
Classification: IACT
waterInactive
Code: 059QF0KO0R
Classification: IACT