Methocarbamol
- Product NDC
- 50090-5006
- 11-digit product format
- 500905006
- Labeler code
- 50090
- Product ID
- 50090-5006_611b863a-9ecd-4c45-b7f5-6f04fabbeadc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040489
- Marketing category
- ANDA
- Marketing start
- 2019-08-15
- 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 |
|---|
| 50090-5006-0 | 50090500600 | 90 TABLET in 1 BOTTLE (50090-5006-0) | 90 tablet | 2020-04-15 | No | No | Historical |