Metaxalone
- Product NDC
- 71205-326
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metaxalone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA203695
- Marketing category
- ANDA
- Substance
- METAXALONE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-326-20 | 20 TABLET in 1 BOTTLE (71205-326-20) | 2020-09-30 | | No | Historical |
| 71205-326-30 | 30 TABLET in 1 BOTTLE (71205-326-30) | 2019-09-01 | | No | Historical |
| 71205-326-60 | 60 TABLET in 1 BOTTLE (71205-326-60) | 2019-09-01 | | No | Historical |
| 71205-326-90 | 90 TABLET in 1 BOTTLE (71205-326-90) | 2019-09-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metaxalone Tablets | Proficient Rx LP | 2024-01-01 | HUMAN PRESCRIPTION DRUG LABEL | 5 |