Details for New Drug Application (NDA): 078737
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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 078737
Tradename: | KETOROLAC TROMETHAMINE |
Applicant: | Sun Pharm |
Ingredient: | ketorolac tromethamine |
Patents: | 0 |
Pharmacology for NDA: 078737
Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 078737
Suppliers and Packaging for NDA: 078737
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
KETOROLAC TROMETHAMINE | ketorolac tromethamine | INJECTABLE;INJECTION | 078737 | ANDA | Sun Pharmaceutical Industries, Inc. | 47335-933 | 47335-933-45 | 25 VIAL, SINGLE-DOSE in 1 CARTON (47335-933-45) / 1 mL in 1 VIAL, SINGLE-DOSE (47335-933-40) |
KETOROLAC TROMETHAMINE | ketorolac tromethamine | INJECTABLE;INJECTION | 078737 | ANDA | Sun Pharmaceutical Industries, Inc. | 47335-934 | 47335-934-45 | 25 VIAL, SINGLE-DOSE in 1 CARTON (47335-934-45) / 1 mL in 1 VIAL, SINGLE-DOSE (47335-934-40) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 15MG/ML | ||||
Approval Date: | Oct 6, 2008 | TE: | AP | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 30MG/ML | ||||
Approval Date: | Oct 6, 2008 | TE: | AP | RLD: | No |
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