Methocarbamol
- Product NDC
- 70518-2209
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK 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 |
|---|
| 70518-2209-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2209-0) | 2019-07-11 | 0000-00-00 | No | Current |
| 70518-2209-1 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2209-1) | 2020-07-29 | 0000-00-00 | No | Current |