Methocarbamol
- Product NDC
- 71335-0828
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208507
- Marketing category
- ANDA
- Substance
- METHOCARBAMOL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71335-0828-4 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0828-4) | 20180115 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 3212f121-9428-4186-8f00-accf08bca473 | Methocarbamol Tablets USP, 500 mg and 750 mg | Bryant Ranch Prepack | 2024-04-04 | HUMAN PRESCRIPTION DRUG LABEL | 6 |