Methocarbamol
- Product NDC
- 72789-428
- 11-digit product format
- 727890428
- Labeler code
- 72789
- Product ID
- 72789-428_4123c4a2-42dd-322b-e063-6294a90a2981
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA040489
- Marketing category
- ANDA
- Marketing start
- 2019-08-15
- 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 |
|---|
| 72789-428-18 | 72789042818 | 18 TABLET in 1 BOTTLE, PLASTIC (72789-428-18) | 18 tablet | 2024-11-20 | No | No | Historical |
| 72789-428-30 | 72789042830 | 30 TABLET in 1 BOTTLE, PLASTIC (72789-428-30) | 30 tablet | 2024-09-12 | No | No | Historical |