Methocarbamol
- Product NDC
- 51407-468
- 11-digit product format
- 514070468
- Labeler code
- 51407
- Product ID
- 51407-468_373a2a8e-23bb-b300-e063-6394a90ad8dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA086988
- Marketing category
- ANDA
- Marketing start
- 1982-01-01
- Substance
- METHOCARBAMOL
- Active strength
- 750 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 125OD7737X | METHOCARBAMOL | 532-03-6 | METHOCARBAMOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51407-468-01 | 51407046801 | 100 TABLET in 1 BOTTLE (51407-468-01) | 100 tablet | 2021-07-07 | No | No | Historical |
| 51407-468-05 | 51407046805 | 500 TABLET in 1 BOTTLE (51407-468-05) | 500 tablet | 2021-07-07 | No | No | Historical |