Methocarbamol
- Product NDC
- 60760-725
- 11-digit product format
- 607600725
- Labeler code
- 60760
- Product ID
- 60760-725_018d9f12-4c65-0f1d-e063-6294a90a348b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- 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 |
|---|
| 60760-725-28 | 60760072528 | 28 TABLET in 1 BOTTLE, PLASTIC (60760-725-28) | 28 tablet | 2023-07-28 | No | No | Historical |
| 60760-725-40 | 60760072540 | 40 TABLET in 1 BOTTLE, PLASTIC (60760-725-40) | 40 tablet | 2019-08-15 | No | No | Historical |
| 60760-725-90 | 60760072590 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-725-90) | 90 tablet | 2023-07-07 | No | No | Historical |