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Last Updated: December 12, 2024

Details for New Drug Application (NDA): 212939


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NDA 212939 describes KETOROLAC TROMETHAMINE, which is a drug marketed by Alembic, Amphastar Pharm, Apotex Inc, Apothecon, Aspiro, Baxter Hlthcare Corp, Bedford, Caplin, Eugia Pharma, Fresenius Kabi Usa, Gland, Gland Pharma Ltd, Hikma, Hospira, Luitpold, Nephron, Sagent Pharms Inc, Sandoz, Steriscience Speclts, Sun Pharm, Wockhardt, Wockhardt Bio Ag, Chartwell Rx, Epic Pharma Llc, Micro Labs Ltd India, Atnahs Pharma Us, Bionpharma, Hetero Labs Ltd Iii, Leading, Mylan, Pliva, Senores Pharms, Teva, Watson Labs, Zydus Lifesciences, and Lupin Ltd, and is included in fifty-six NDAs. It is available from sixty-four suppliers. Additional details are available on the KETOROLAC TROMETHAMINE profile page.

The generic ingredient in KETOROLAC TROMETHAMINE is ketorolac tromethamine; phenylephrine hydrochloride. There are eighteen drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the ketorolac tromethamine; phenylephrine hydrochloride profile page.
Summary for 212939
Tradename:KETOROLAC TROMETHAMINE
Applicant:Eugia Pharma
Ingredient:ketorolac tromethamine
Patents:0
Pharmacology for NDA: 212939
Mechanism of ActionCyclooxygenase Inhibitors
Medical Subject Heading (MeSH) Categories for 212939
Suppliers and Packaging for NDA: 212939
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
KETOROLAC TROMETHAMINE ketorolac tromethamine INJECTABLE;INJECTION 212939 ANDA Eugia US LLC 55150-339 55150-339-01 1 VIAL, SINGLE-DOSE in 1 CARTON (55150-339-01) / 1 mL in 1 VIAL, SINGLE-DOSE
KETOROLAC TROMETHAMINE ketorolac tromethamine INJECTABLE;INJECTION 212939 ANDA Eugia US LLC 55150-339 55150-339-25 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-339-25) / 1 mL in 1 VIAL, SINGLE-DOSE

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrength15MG/ML
Approval Date:Oct 20, 2020TE:RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrength30MG/ML
Approval Date:Oct 20, 2020TE:RLD:No

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