Product NDC: | 52125-526 |
Proprietary Name: | Ketorolac Tromethamine |
Non Proprietary Name: | ketorolac tromethamine |
Active Ingredient(s): | 5 mg/1 & nbsp; ketorolac tromethamine |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52125-526 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078434 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130415 |
Package NDC: | 52125-526-01 |
Package Description: | 1 SOLUTION in 1 CARTON (52125-526-01) |
NDC Code | 52125-526-01 |
Proprietary Name | Ketorolac Tromethamine |
Package Description | 1 SOLUTION in 1 CARTON (52125-526-01) |
Product NDC | 52125-526 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ketorolac tromethamine |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20130415 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | KETOROLAC TROMETHAMINE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |