Methocarbamol
- Product NDC
- 68788-7809
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA208507
- Marketing category
- ANDA
- Substance
- METHOCARBAMOL
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68788-7809-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7809-1) | 2020-10-29 | 0000-00-00 | No | Current |
| 68788-7809-2 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-7809-2) | 2020-10-29 | 0000-00-00 | No | Current |
| 68788-7809-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7809-3) | 2020-10-29 | 0000-00-00 | No | Current |
| 68788-7809-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7809-6) | 2020-10-29 | 0000-00-00 | No | Current |
| 68788-7809-8 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-7809-8) | 2020-10-29 | 0000-00-00 | No | Current |
| 68788-7809-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7809-9) | 2020-10-29 | 0000-00-00 | No | Current |