Product NDC: | 21695-463 |
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 |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-463 |
Labeler Name: | Rebel Distributors Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019700 |
Marketing Category: | NDA |
Start Marketing Date: | 19921109 |
Package NDC: | 21695-463-05 |
Package Description: | 5 mL in 1 BOTTLE (21695-463-05) |
NDC Code | 21695-463-05 |
Proprietary Name | ACULAR |
Package Description | 5 mL in 1 BOTTLE (21695-463-05) |
Product NDC | 21695-463 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | KETOROLAC TROMETHAMINE |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 19921109 |
Marketing Category Name | NDA |
Labeler Name | Rebel Distributors Corp. |
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] |