Methocarbamol
- Product NDC
- 68788-8822
- 11-digit product format
- 687888822
- Labeler code
- 68788
- Product ID
- 68788-8822_eed9ebd1-c243-4e82-bf4e-5fec370e722e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090200
- Marketing category
- ANDA
- Marketing start
- 2025-02-10
- Substance
- METHOCARBAMOL
- Active strength
- 500 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 |
|---|
| 68788-8822-1 | 68788882201 | 100 TABLET in 1 BOTTLE (68788-8822-1) | 100 tablet | 2025-02-10 | No | No | Historical |
| 68788-8822-2 | 68788882202 | 20 TABLET in 1 BOTTLE (68788-8822-2) | 20 tablet | 2025-02-10 | No | No | Historical |
| 68788-8822-3 | 68788882203 | 30 TABLET in 1 BOTTLE (68788-8822-3) | 30 tablet | 2025-02-10 | No | No | Historical |
| 68788-8822-4 | 68788882204 | 40 TABLET in 1 BOTTLE (68788-8822-4) | 40 tablet | 2025-02-10 | No | No | Historical |
| 68788-8822-6 | 68788882206 | 60 TABLET in 1 BOTTLE (68788-8822-6) | 60 tablet | 2025-02-10 | No | No | Historical |
| 68788-8822-8 | 68788882208 | 120 TABLET in 1 BOTTLE (68788-8822-8) | 120 tablet | 2025-02-10 | No | No | Historical |
| 68788-8822-9 | 68788882209 | 90 TABLET in 1 BOTTLE (68788-8822-9) | 90 tablet | 2025-02-10 | No | No | Historical |