Methocarbamol
- Product NDC
- 67296-1662
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, 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 |
|---|
| 67296-1662-7 | 15 TABLET, FILM COATED in 1 BOTTLE (67296-1662-7) | 2019-01-01 | 0000-00-00 | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| methocarbamol 750mg | RedPharm Drug, Inc. | 2024-08-03 | HUMAN PRESCRIPTION DRUG LABEL | 3 |