| Product NDC: | 41616-220 |
| 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: | 41616-220 |
| Labeler Name: | Sun Pharma Global Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090017 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091106 |
| Package NDC: | 41616-220-90 |
| Package Description: | 5 mL in 1 BOTTLE (41616-220-90) |
| NDC Code | 41616-220-90 |
| Proprietary Name | Ketorolac Tromethamine |
| Package Description | 5 mL in 1 BOTTLE (41616-220-90) |
| Product NDC | 41616-220 |
| 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] |