Product NDC: | 0023-2181 |
Proprietary Name: | Acular |
Non Proprietary Name: | Ketorolac Tromethamine |
Active Ingredient(s): | 5 mg/mL & nbsp; Ketorolac Tromethamine |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0023-2181 |
Labeler Name: | Allergan, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019700 |
Marketing Category: | NDA |
Start Marketing Date: | 19921201 |
Package NDC: | 0023-2181-05 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0023-2181-05) > 5 mL in 1 BOTTLE, DROPPER |
NDC Code | 0023-2181-05 |
Proprietary Name | Acular |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0023-2181-05) > 5 mL in 1 BOTTLE, DROPPER |
Product NDC | 0023-2181 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ketorolac Tromethamine |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | OPHTHALMIC |
Start Marketing Date | 19921201 |
Marketing Category Name | NDA |
Labeler Name | Allergan, 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] |