NDC 70518-0896-2 - Aripiprazole
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
- 70518-0896
- Requested NDC
- 70518-0896-2
- Package NDCs from labels
- 70518-0896-0, 70518-0896-2, 70518-0896-1
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2024-01-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Aripiprazole - REMEDYREPACK INC. | REMEDYREPACK INC. | 2024-01-23 | HUMAN PRESCRIPTION DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| Aripiprazole | ARIPIPRAZOLE | Exelan Pharmaceuticals, Inc. | 705190bf-9f9d-4183-a56b-4eeafeacde59 | 2018-12-28 | Boxed warning, Warnings, Adverse reactions | 349547 349553 602964 349545 349490 402131 82VFR53I78 |
| ARIPIPRAZOLE | ARIPIPRAZOLE | Camber Pharmaceuticals, Inc. | 3718e585-06b9-40fd-a3eb-18b6497a4235 | 2017-08-08 | Boxed warning, Warnings, Adverse reactions | 349547 349553 602964 349545 349490 402131 82VFR53I78 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.