Product NDC: | 41616-221 |
Proprietary Name: | Ketorolac Tromethamine |
Non Proprietary Name: | Ketorolac Tromethamine |
Active Ingredient(s): | 5 mg/mL & nbsp; Ketorolac Tromethamine |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41616-221 |
Labeler Name: | Sun Pharma Global Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090017 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091106 |
Package NDC: | 41616-221-90 |
Package Description: | 10 mL in 1 BOTTLE (41616-221-90) |
NDC Code | 41616-221-90 |
Proprietary Name | Ketorolac Tromethamine |
Package Description | 10 mL in 1 BOTTLE (41616-221-90) |
Product NDC | 41616-221 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ketorolac Tromethamine |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20091106 |
Marketing Category Name | ANDA |
Labeler Name | Sun Pharma Global Inc. |
Substance Name | KETOROLAC TROMETHAMINE |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |