Methocarbamol Tablets, USP, 750 mg
- Product NDC
- 72162-2488
- 11-digit product format
- 721622488
- Labeler code
- 72162
- Product ID
- 72162-2488_346ba3fe-736a-b3d6-e063-6394a90a955f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212623
- Marketing category
- ANDA
- Marketing start
- 2024-01-01
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2488-1 | 72162248801 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2488-1) | 2025-05-05 | No | No | Historical |
| 72162-2488-5 | 72162248805 | 500 TABLET, FILM COATED in 1 BOTTLE (72162-2488-5) | 2025-05-05 | No | No | Historical |