Methocarbamol
- Product NDC
- 45865-987
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- medsource pharmaceuticals
- Application
- ANDA208507
- Marketing category
- ANDA
- Substance
- METHOCARBAMOL
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 45865-987-60 | 60 TABLET, FILM COATED in 1 BOTTLE (45865-987-60) | 2019-12-11 | 0000-00-00 | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Methocarbamol Tablets USP, 500 mg | medsource pharmaceuticals | Beximco Pharmaceuticals USA Inc. | 2019-12-30 | HUMAN PRESCRIPTION DRUG LABEL | 1 |