| Product NDC: | 61314-018 |
| Proprietary Name: | KETOROLAC TROMETHAMINE |
| Non Proprietary Name: | ketorolac tromethamine |
| Active Ingredient(s): | 4 mg/mL & nbsp; ketorolac tromethamine |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 61314-018 |
| Labeler Name: | Falcon Pharmaceuticals, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078721 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091105 |
| Package NDC: | 61314-018-05 |
| Package Description: | 5 mL in 1 BOTTLE (61314-018-05) |
| NDC Code | 61314-018-05 |
| Proprietary Name | KETOROLAC TROMETHAMINE |
| Package Description | 5 mL in 1 BOTTLE (61314-018-05) |
| Product NDC | 61314-018 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ketorolac tromethamine |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20091105 |
| Marketing Category Name | ANDA |
| Labeler Name | Falcon Pharmaceuticals, Ltd. |
| Substance Name | KETOROLAC TROMETHAMINE |
| Strength Number | 4 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |