NDC 70518-3548-01 - Rexulti
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
- 70518-3548
- Requested NDC
- 70518-3548-01
- Package NDCs from labels
- 70518-3548-0, 70518-3548-2, 70518-3548-1, 70518-3548-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-06-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Rexulti - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-06-02 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-3548-0 | Rexulti | 30 in 1 BOTTLE | TABLET | 30 | 5 | |
| 70518-3548-0 | Rexulti | 1 in 1 CARTON | TABLET | 1 | 5 | |
| 70518-3548-1 | Rexulti | 50 in 1 BOX | TABLET | 50 | 5 | |
| 70518-3548-2 | Rexulti | 1 in 1 POUCH | TABLET | 1 | 5 |
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 |
|---|---|---|---|---|---|---|
| Renewal Firming Day Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | BURT'S BEES, INC. | 18ceb5d8-4b76-6a54-e054-00144ff88e88 | 2015-06-18 | Warnings | 15FIX9V2JP |
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD. | 30468afc-9616-4765-b046-12e97a0a7827 | 2010-12-20 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.