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Ketorolac Tromethamine
Ketorolac Tromethamine - 0641-6042-25 - (Ketorolac Tromethamine)
Drug Information of Ketorolac Tromethamine
| Product NDC: | 0641-6042 |
| Proprietary Name: | Ketorolac Tromethamine |
| Non Proprietary Name: | Ketorolac Tromethamine |
| Active Ingredient(s): | 30 mg/mL & nbsp; Ketorolac Tromethamine |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ketorolac Tromethamine
| Product NDC: | 0641-6042 |
| Labeler Name: | West-ward Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075772 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040721 |
Package Information of Ketorolac Tromethamine
| Package NDC: | 0641-6042-25 |
| Package Description: | 25 VIAL in 1 CARTON (0641-6042-25) > 1 mL in 1 VIAL (0641-6042-01) |
NDC Information of Ketorolac Tromethamine
| NDC Code | 0641-6042-25 |
| Proprietary Name | Ketorolac Tromethamine |
| Package Description | 25 VIAL in 1 CARTON (0641-6042-25) > 1 mL in 1 VIAL (0641-6042-01) |
| Product NDC | 0641-6042 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ketorolac Tromethamine |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| 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] |
