Methocarbamol
- Product NDC
- 70934-230
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind 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 |
|---|
| 70934-230-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-230-20) | 2019-01-10 | 0000-00-00 | No | Current |
| 70934-230-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-230-30) | 2019-01-10 | 0000-00-00 | No | Current |