NDC 80425-0139-01 - Ketorolac Tromethamine
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 80425-0139
- Requested NDC
- 80425-0139-01
- Package NDCs from labels
- 80425-0139-1, 80425-0139-3, 80425-0139-2, 80425-0139-01
- Manufacturer
- Advanced Rx Pharmacy of Tennessee, LLC
- Effective date
- 2024-12-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ketorolac Tromethamine - Advanced Rx Pharmacy of Tennessee, LLC | Advanced Rx Pharmacy of Tennessee, LLC | 2024-12-31 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80425-0139-1 | Ketorolac Tromethamine | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 5 | |
| 80425-0139-2 | Ketorolac Tromethamine | 9 in 1 BOTTLE | TABLET, FILM COATED | 9 | 5 | |
| 80425-0139-3 | Ketorolac Tromethamine | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 80425-0139 | KETOROLAC TROMETHAMINE TABLET, FILM COATED [ADVANCED RX PHARMACY OF TENNESSEE, LLC] | 5 | Current NDC, Legacy NDC, 3 package rows | 20250101_c1717245-cef3-b3d7-e053-2a95a90a1ac5.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 80425-0139-1 | EA - Each | 80425-0139 | 70add81b-d8f5-4118-b5c1-05bf84165ade | 1 | 2023-06-06 |
| 80425-0139-2 | EA - Each | 80425-0139 | 0b665173-2504-4c55-b5a5-980fa83937b7 | 1 | 2023-06-06 |
| 80425-0139-3 | EA - Each | 80425-0139 | fcf73ba8-2e41-4714-89c3-f0dc2d794b1e | 1 | 2023-06-06 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | Preferred Pharmaceuticals Inc. | 18b450d2-e715-4710-a1d8-22b782f87f9c | 2025-09-23 | Boxed warning, Warnings, Adverse reactions | 834022 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | ProPharma Distribution | 3f2956d9-9e68-f35e-e063-6394a90a706d | 2025-09-18 | Boxed warning, Warnings, Adverse reactions | 4EVE5946BQ |
| Acular | KETOROLAC TROMETHAMINE | Allergan, Inc. | c94644d3-7b64-4f3d-a0c7-12c77466a0fc | 2025-09-18 | Warnings, Adverse reactions | 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | American Health Packaging | 48244614-53ec-47e6-ad48-50814bdcceb7 | 2025-08-28 | Boxed warning, Warnings, Adverse reactions | ANDA074754 834022 4EVE5946BQ |
| KETOROLAC TROMETHAMINE | KETOROLAC TROMETHAMINE | HF Acquisition Co LLC, DBA HealthFirst | 3d746288-681a-5232-e063-6394a90afabd | 2025-08-28 | Boxed warning, Warnings, Adverse reactions | 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | A-S Medication Solutions | 0952d430-2665-4952-ba06-ab99f054f4df | 2025-08-26 | Boxed warning, Warnings, Adverse reactions | 834022 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | NuCare Pharmaceuticals, Inc. | 3b3cc67c-e1ff-3a0a-e063-6394a90adb9a | 2025-07-31 | Warnings, Adverse reactions | 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | Redpharm Drug | 3b0aaf7f-c2fe-83c6-e063-6294a90a6f27 | 2025-07-29 | Boxed warning, Warnings, Adverse reactions | 834022 4EVE5946BQ |
| KETOROLAC TROMETHAMINE | KETOROLAC TROMETHAMINE | PD-Rx Pharmaceuticals, Inc. | 862dd7b7-8ed5-42bf-870e-a45b86740226 | 2025-07-17 | Boxed warning, Warnings, Adverse reactions | 834022 4EVE5946BQ |
| Ketorolac tromethamine | KETOROLAC TROMETHAMINE | Henry Schein, Inc. | 99c06dde-f218-4d81-91e0-f37a748872d6 | 2025-07-14 | Boxed warning, Warnings, Adverse reactions | 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | Bryant Ranch Prepack | afc691f8-517a-4d88-8322-87dafec8f064 | 2025-06-23 | Boxed warning, Warnings, Adverse reactions | 834022 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | Henry Schein, Inc. | 1e65d11b-5aa9-4a6b-b5d6-c19828748fea | 2025-06-20 | Boxed warning, Warnings, Adverse reactions | 4EVE5946BQ |
| Ketorolac tromethamine | KETOROLAC TROMETHAMINE | Henry Schein, Inc. | 606b0f2f-de28-42a9-96f4-cacba2c7c56a | 2025-06-19 | Boxed warning, Warnings, Adverse reactions | 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | Bryant Ranch Prepack | 8f36fde8-bc59-4a59-8659-b173cfd15774 | 2025-05-15 | Boxed warning, Warnings, Adverse reactions | 834022 4EVE5946BQ |
| ketorolac tromethamine | KETOROLAC TROMETHAMINE | NuCare Pharmaceuticals,Inc. | fe7eb195-48be-753b-e053-6294a90a8500 | 2025-04-25 | Boxed warning, Warnings, Adverse reactions | 834022 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | PD-Rx Pharmaceuticals, Inc. | add10ccd-c205-4512-9619-253290fa1152 | 2025-03-12 | Boxed warning, Warnings, Adverse reactions | ANDA074754 834022 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | Bionpharma Inc. | eda4b884-527c-42d3-971b-4d1678e5adbf | 2025-03-05 | Boxed warning, Warnings, Adverse reactions | 834022 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | Golden State Medical Supply, Inc. | ec6d453b-4b84-53d4-e053-2995a90a6006 | 2025-02-24 | Boxed warning, Warnings, Adverse reactions | 834022 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | Ajanta Pharma USA Inc. | 36713fb3-d301-432d-a95d-06e368fc8a22 | 2025-02-13 | Boxed warning, Warnings, Adverse reactions | 834022 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | A-S Medication Solutions | 9fdba2e6-969f-4624-b08b-a42f99e4eff9 | 2025-02-06 | Boxed warning, Warnings, Adverse reactions | ANDA074754 834022 4EVE5946BQ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.