Methocarbamol
- Product NDC
- 55700-716
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA208507
- Marketing category
- ANDA
- Substance
- METHOCARBAMOL
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 55700-716-01 | 120 TABLET, FILM COATED in 1 BOTTLE (55700-716-01) | 2019-02-08 | 0000-00-00 | No | Current |
| 55700-716-20 | 20 TABLET, FILM COATED in 1 BOTTLE (55700-716-20) | 2019-01-11 | 0000-00-00 | No | Current |
| 55700-716-30 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-716-30) | 2019-01-11 | 0000-00-00 | No | Current |
| 55700-716-60 | 60 TABLET, FILM COATED in 1 BOTTLE (55700-716-60) | 2019-01-11 | 0000-00-00 | No | Current |
| 55700-716-90 | 90 TABLET, FILM COATED in 1 BOTTLE (55700-716-90) | 2019-01-11 | 0000-00-00 | No | Current |