NDC 70518-0048-06 - 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
- 70518-0048
- Requested NDC
- 70518-0048-06
- Package NDCs from labels
- 70518-0048-0, 70518-0048-1, 70518-0048-2, 70518-0048-3, 70518-0048-4, 70518-0048-5, 70518-0048-6, 70518-0048-06
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-06-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ketorolac Tromethamine Tablets USP, 10 mg Rx only | REMEDYREPACK INC. | 2026-06-22 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-0048-0 | Ketorolac Tromethamine | 25 in 1 BOTTLE | TABLET, FILM COATED | 25 | 25 | |
| 70518-0048-1 | Ketorolac Tromethamine | 1 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 1 | 25 | |
| 70518-0048-2 | Ketorolac Tromethamine | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 25 | |
| 70518-0048-3 | Ketorolac Tromethamine | 8 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 8 | 25 | |
| 70518-0048-4 | Ketorolac Tromethamine | 20 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 20 | 25 | |
| 70518-0048-5 | Ketorolac Tromethamine | 10 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 10 | 25 | |
| 70518-0048-6 | Ketorolac Tromethamine | 12 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 12 | 25 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-0048 | KETOROLAC TROMETHAMINE TABLET, FILM COATED [REMEDYREPACK INC.] | 20 | Current NDC, Legacy NDC, 7 package rows | 20250529_f47d4365-40a8-445b-99cd-49edad6a8ffc.zip |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.