warnings
WARNINGS Metaxalone may enhance the effects of alcohol and other CNS depressants.
Metaxalone
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Metaxalone
- Generic name
- METAXALONE
- Manufacturer
- Proficient Rx LP
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 9c7d0cd4-625a-485e-9d13-ce854630148c
- SPL ID
- 4083545a-a990-4820-a601-06a7d8a31a35
- Version
- 4
- Effective date
- 2024-03-01
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:52:52
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 207466 | derived:openfda.application_number |
| application number | ANDA207466 | openfda.application_number | |
| brand name | Metaxalone | openfda.brand_name | |
| generic name | METAXALONE | openfda.generic_name | |
| manufacturer name | Proficient Rx LP | openfda.manufacturer_name | |
| ndc | package | 71205-016-30 | openfda.package_ndc |
| ndc | package | 71205-016-90 | openfda.package_ndc |
| ndc | package | 71205-016-60 | openfda.package_ndc |
| ndc | package | 71205-016-10 | openfda.package_ndc |
| ndc | product | 71205-016 | openfda.product_ndc |
| ndc11 | package | 71205001660 | derived:openfda.package_ndc |
| ndc11 | package | 71205001690 | derived:openfda.package_ndc |
| ndc11 | package | 71205001630 | derived:openfda.package_ndc |
| ndc11 | package | 71205001610 | derived:openfda.package_ndc |
| rxcui | 351254 | openfda.rxcui | |
| spl id | 4083545a-a990-4820-a601-06a7d8a31a35 | id | |
| spl set id | 9c7d0cd4-625a-485e-9d13-ce854630148c | set_id | |
| unii | 1NMA9J598Y | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS The most frequent reactions to metaxalone include: CNS: drowsiness, dizziness, headache, and nervousness or “irritability”; Digestive: nausea, vomiting, gastrointestinal upset. Other adverse reactions are: Immune System: hypersensitivity reaction, rash with or without pruritus; Hematologic: leukopenia; hemolytic anemia; Hepatobiliary: jaundice. Though rare, anaphylactoid reactions have been reported with metaxalone. To report SUSPECTED ADVERSE REACTIONS, contact Dr.Reddy’s Laboratories, Inc., at 1-888-375-3784 or FDA at 1-800-FDA-1088 or http://www.fda.gov/medwatch
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.