Product NDC: | 0641-6043 |
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: | 0641-6043 |
Labeler Name: | West-ward Pharmaceutical Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075772 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040721 |
Package NDC: | 0641-6043-25 |
Package Description: | 25 VIAL in 1 CARTON (0641-6043-25) > 2 mL in 1 VIAL (0641-6043-01) |
NDC Code | 0641-6043-25 |
Proprietary Name | Ketorolac Tromethamine |
Package Description | 25 VIAL in 1 CARTON (0641-6043-25) > 2 mL in 1 VIAL (0641-6043-01) |
Product NDC | 0641-6043 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ketorolac Tromethamine |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 20040721 |
Marketing Category Name | ANDA |
Labeler Name | West-ward Pharmaceutical Corp. |
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] |