Metaxalone
- Product NDC
- 71205-470
- 11-digit product format
- 712050470
- Labeler code
- 71205
- Product ID
- 71205-470_9bf5fd84-b077-461f-96d2-b3e67247700a
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71205-470-60 | EA - Each | 71205-470 | dda9b351-97f9-48c2-87ce-f52dae96e352 | 1 | 2021-04-08 |
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 71205-470-30 | 71205047030 | 30 TABLET in 1 BOTTLE (71205-470-30) | 30 tablet | 2020-08-24 | 0000-00-00 | No | No | Current |
| 71205-470-60 | 71205047060 | 60 TABLET in 1 BOTTLE (71205-470-60) | 60 tablet | 2020-08-24 | 0000-00-00 | No | No | Current |
| 71205-470-90 | 71205047090 | 90 TABLET in 1 BOTTLE (71205-470-90) | 90 tablet | 2020-08-24 | 0000-00-00 | No | No | Current |