NDC 70518-0831-2 - Haloperidol
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
- 70518-0831
- Requested NDC
- 70518-0831-2
- Package NDCs from labels
- 70518-0831-0, 70518-0831-2, 70518-0831-1
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2023-04-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Haloperidol Tablets, USP | REMEDYREPACK INC. | 2023-04-05 | 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 |
|---|---|---|---|---|---|---|
| Haloperidol | HALOPERIDOL | Bryant Ranch Prepack | 1171bd60-7105-4b70-a24c-f2bc8c52a8c0 | 2024-01-11 | Boxed warning, Warnings, Adverse reactions | 310671 J6292F8L3D |
| Haloperidol | HALOPERIDOL | Bryant Ranch Prepack | a79c12f2-cf98-4337-8b6a-7b9ef2afa9d5 | 2024-01-11 | Boxed warning, Warnings, Adverse reactions | 197754 J6292F8L3D |
| Haloperidol | HALOPERIDOL | Amici Pharmaceuticals, LLC | 9a9e20dd-646a-4fe9-a345-1b5bda8e7775 | 2022-05-02 | Boxed warning, Warnings, Adverse reactions | 314035 314034 310670 310672 310671 197754 J6292F8L3D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.