NDC 70518-4559-01 - Metaxalone
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
- 70518-4559
- Requested NDC
- 70518-4559-01
- Package NDCs from labels
- 70518-4559-0, 70518-4559-1, 70518-4559-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-08-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Metaxalone - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-08-26 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-4559-0 | Metaxalone | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | 1 |
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 |
|---|---|---|---|---|---|---|
| Metaxalone | METAXALONE | Asclemed USA, Inc. | 02c42f72-5d78-436d-8105-8c0f8d4c0d91 | 2022-07-25 | Warnings, Adverse reactions | 351254 1NMA9J598Y |
| Metaxalone | METAXALONE | Proficient Rx LP | ee86f52c-fbf4-4882-bb7d-50220736fbb3 | 2022-04-01 | Warnings, Adverse reactions | 351254 1NMA9J598Y |
| Metaxalone | METAXALONE | Doc Rx | 4a558a2f-f9be-40d1-8d02-dd0c8c501ef6 | 2022-03-24 | Warnings, Adverse reactions | 351254 1NMA9J598Y |
| Metaxalone | METAXALONE | Doc Rx | 87518046-c959-d5f3-e053-2a95a90a5f7e | 2021-09-28 | Warnings, Adverse reactions | 351254 1NMA9J598Y |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.