Metaxalone
- Product NDC
- 71205-961
- 11-digit product format
- 712050961
- Labeler code
- 71205
- Product ID
- 71205-961_1a641881-7f74-4619-bb54-5030bdb79fc1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metaxalone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA208774
- Marketing category
- ANDA
- Marketing start
- 2018-09-24
- Marketing end
- 0000-00-00
- Substance
- METAXALONE
- Active strength
- 800 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-961-00 | 71205096100 | 100 TABLET in 1 BOTTLE (71205-961-00) | 100 tablet | 2020-07-31 | 0000-00-00 | No | No | Current |
| 71205-961-30 | 71205096130 | 30 TABLET in 1 BOTTLE (71205-961-30) | 30 tablet | 2020-07-31 | 0000-00-00 | No | No | Current |
| 71205-961-55 | 71205096155 | 500 TABLET in 1 BOTTLE (71205-961-55) | 500 tablet | 2020-07-31 | 0000-00-00 | No | No | Current |
| 71205-961-60 | 71205096160 | 60 TABLET in 1 BOTTLE (71205-961-60) | 60 tablet | 2020-07-31 | 0000-00-00 | No | No | Current |
| 71205-961-72 | 71205096172 | 120 TABLET in 1 BOTTLE (71205-961-72) | 120 tablet | 2020-07-31 | 0000-00-00 | No | No | Current |
| 71205-961-90 | 71205096190 | 90 TABLET in 1 BOTTLE (71205-961-90) | 90 tablet | 2020-07-31 | 0000-00-00 | No | No | Current |