Product NDC: | 49349-737 |
Proprietary Name: | Ketorolac Tromethamine |
Non Proprietary Name: | KETOROLAC TROMETHAMINE |
Active Ingredient(s): | 10 mg/1 & nbsp; KETOROLAC TROMETHAMINE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49349-737 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074754 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120904 |
Package NDC: | 49349-737-50 |
Package Description: | 40 TABLET in 1 VIAL (49349-737-50) |
NDC Code | 49349-737-50 |
Proprietary Name | Ketorolac Tromethamine |
Package Description | 40 TABLET in 1 VIAL (49349-737-50) |
Product NDC | 49349-737 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | KETOROLAC TROMETHAMINE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120904 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | KETOROLAC TROMETHAMINE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |