Ketorolac Tromethamine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Apotheca, Inc. The primary component is Ketorolac Tromethamine.
| Product ID | 12634-809_69956c5a-014b-4e75-b4c1-6e51d7e80315 | 
| NDC | 12634-809 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | Ketorolac Tromethamine | 
| Generic Name | Ketorolac Tromethamine | 
| Dosage Form | Tablet | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2005-10-25 | 
| Marketing Category | ANDA / ANDA | 
| Application Number | ANDA074754 | 
| Labeler Name | Apotheca, Inc | 
| Substance Name | KETOROLAC TROMETHAMINE | 
| Active Ingredient Strength | 10 mg/1 | 
| Pharm Classes | Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC],Cyclooxygenase Inhibitor [EPC] | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2019-12-31 | 
| Marketing Start Date | 2005-10-25 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA074754 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2005-10-25 | 
| Inactivation Date | 2020-01-31 | 
| Ingredient | Strength | 
|---|---|
| KETOROLAC TROMETHAMINE | 10 mg/1 | 
| SPL SET ID: | e20df5b6-84da-4715-b36e-bb7e4be55416 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0093-0314 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 0338-0069 | KETOROLAC TROMETHAMINE | ketorolac tromethamine | 
| 0338-0072 | KETOROLAC TROMETHAMINE | ketorolac tromethamine | 
| 0338-0076 | KETOROLAC TROMETHAMINE | ketorolac tromethamine | 
| 0378-1134 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 0409-3796 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 0409-3793 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 0409-3795 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 68071-1787 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 68071-1785 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 68083-132 | ketorolac tromethamine | ketorolac tromethamine | 
| 68083-104 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 68083-134 | ketorolac tromethamine | ketorolac tromethamine | 
| 68083-103 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 68071-4811 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 68083-133 | ketorolac tromethamine | ketorolac tromethamine | 
| 68151-0098 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 68387-440 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 0517-0902 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 0517-0801 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 68788-9321 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 0517-0601 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 68788-7384 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 68788-9205 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 69543-386 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 69543-407 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 0548-9021 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 69543-388 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 69543-405 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 70518-0048 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 70518-1091 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 70518-1165 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 70518-1159 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 70518-1669 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 70518-1239 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 70518-1074 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 70518-1340 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 70518-1889 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 70860-700 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 70860-701 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 70934-029 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 71205-116 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 71872-7131 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 71872-7022 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 71872-7118 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 71872-7119 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 71872-7132 | Ketorolac Tromethamine | Ketorolac Tromethamine | 
| 72266-118 | ketorolac tromethamine | ketorolac tromethamine | 
| 72266-119 | ketorolac tromethamine | ketorolac tromethamine | 
| 76045-104 | Ketorolac Tromethamine | Ketorolac Tromethamine |