Methocarbamol
- Product NDC
- 50090-4793
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA208507
- Marketing category
- ANDA
- Substance
- METHOCARBAMOL
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 50090-4793-0 | 40 TABLET, FILM COATED in 1 BOTTLE (50090-4793-0) | 2019-12-12 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Methocarbamol Tablets USP, 500 mg and 750 mg | A-S Medication Solutions | 2025-07-16 | HUMAN PRESCRIPTION DRUG LABEL | 6 |