Product NDC: | 49349-837 |
Proprietary Name: | KETOROLAC TROMETHAMINE |
Non Proprietary Name: | KETOROLAC TROMETHAMINE |
Active Ingredient(s): | 30 mg/mL & nbsp; KETOROLAC TROMETHAMINE |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49349-837 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077942 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130614 |
Package NDC: | 49349-837-41 |
Package Description: | 1 mL in 1 VIAL (49349-837-41) |
NDC Code | 49349-837-41 |
Proprietary Name | KETOROLAC TROMETHAMINE |
Package Description | 1 mL in 1 VIAL (49349-837-41) |
Product NDC | 49349-837 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | KETOROLAC TROMETHAMINE |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 20130614 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | KETOROLAC TROMETHAMINE |
Strength Number | 30 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |