Methocarbamol
- Product NDC
- 67296-1435
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Redpharm Drug, Inc.
- Application
- ANDA040489
- Marketing category
- ANDA
- Substance
- METHOCARBAMOL
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 67296-1435-1 | 15 TABLET in 1 BOTTLE (67296-1435-1) | 2019-08-15 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Methocarbamol Tablets, USP 500 mg Methocarbamol Tablets, USP 750 mg Rx Only | Redpharm Drug, Inc. | 2025-01-23 | HUMAN PRESCRIPTION DRUG LABEL | 3 |
| Methocarbamol Tablets, USP 500 mg Methocarbamol Tablets, USP 750 mg Rx Only | Redpharm Drug, Inc. | 2023-02-06 | HUMAN PRESCRIPTION DRUG LABEL | 1 |