NDC 80425-0267-01 - 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
- 80425-0267
- Requested NDC
- 80425-0267-01
- Package NDCs from labels
- 80425-0267-1, 80425-0267-2, 80425-0267-3, 80425-0267-4, 80425-0267-5, 80425-0267-01
- 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 |
|---|---|---|---|---|---|---|
| 80425-0267-1 | Ketorolac Tromethamine | 9 in 1 BOTTLE | TABLET, FILM COATED | 9 | 3 | |
| 80425-0267-2 | Ketorolac Tromethamine | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | 3 | |
| 80425-0267-3 | Ketorolac Tromethamine | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 3 | |
| 80425-0267-4 | Ketorolac Tromethamine | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | 3 | |
| 80425-0267-5 | Ketorolac Tromethamine | 10 in 1 BOTTLE | TABLET, FILM COATED | 10 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 80425-0267 | KETOROLAC TROMETHAMINE TABLET, FILM COATED [ADVANCED RX PHARMACY OF TENNESSEE, LLC] | 3 | Current NDC, 5 package rows | 20250102_f4e7f1c8-e458-0860-e053-2a95a90a1bf0.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 80425-0267-1 | EA - Each | 80425-0267 | 7f333244-4aa6-487e-9bfa-3c425d655b2f | 1 | 2023-04-07 |
| 80425-0267-2 | EA - Each | 80425-0267 | 44667709-05c6-4da2-bdda-fffbed00dfa1 | 1 | 2023-04-07 |
| 80425-0267-3 | EA - Each | 80425-0267 | 0b79c085-7336-4a3b-aecf-f92f2256cbd0 | 1 | 2023-04-07 |
| 80425-0267-4 | EA - Each | 80425-0267 | 89140c3e-8295-4419-960c-9f33244ecd3f | 1 | 2023-04-07 |
| 80425-0267-5 | EA - Each | 80425-0267 | 58a927a8-9ee5-408c-aa6c-a943444b53e5 | 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 | Proficient Rx LP | 014ba8d7-7ed3-4d4a-847a-22b65161117e | 2021-07-01 | Boxed warning, Warnings, Adverse reactions | 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | Proficient Rx LP | fc8ba956-4d3d-4f52-ac8e-89d52a480b48 | 2021-06-01 | Warnings, Adverse reactions | 4EVE5946BQ |
| Ketorolac Tromethamine | KETOROLAC TROMETHAMINE | Sun Pharmaceutical Industries, Inc. | 2c76b8f9-5385-4c98-aebb-bdca8613d24b | 2018-10-24 | Warnings, Adverse reactions | 4EVE5946BQ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.