Methocarbamol
- Product NDC
- 68071-2513
- 11-digit product format
- 680712513
- Labeler code
- 68071
- Product ID
- 68071-2513_ca505dbe-1211-619b-e053-2a95a90a62ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA040489
- Marketing category
- ANDA
- Marketing start
- 2019-08-15
- Marketing end
- 0000-00-00
- Substance
- METHOCARBAMOL
- Active strength
- 750 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2513-2 | 68071251302 | 20 TABLET in 1 BOTTLE (68071-2513-2) | 20 tablet | 2021-08-24 | 0000-00-00 | No | No | Current |
| 68071-2513-3 | 68071251303 | 30 TABLET in 1 BOTTLE (68071-2513-3) | 30 tablet | 2021-08-24 | 0000-00-00 | No | No | Current |