Methocarbamol
- Product NDC
- 70518-4472
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA086988
- Marketing category
- ANDA
- Substance
- METHOCARBAMOL
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 70518-4472-0 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-4472-0) | 2025-09-09 | No | Historical | |
| 70518-4472-1 | 60 TABLET in 1 BOTTLE, PLASTIC (70518-4472-1) | 2025-09-09 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Methocarbamol Tablets, USP | REMEDYREPACK INC. | 2025-09-09 | HUMAN PRESCRIPTION DRUG LABEL | 1 |