Methocarbamol
- Product NDC
- 60687-568
- 11-digit product format
- 606870568
- Labeler code
- 60687
- Product ID
- 60687-568_22058b66-8c4a-4a0b-e063-6394a90ae73e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA090200
- Marketing category
- ANDA
- Marketing start
- 2020-05-20
- 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 |
|---|
| 60687-568-01 | 60687056801 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-568-01) / 1 TABLET in 1 BLISTER PACK (60687-568-11) | 100 blister pack | 2020-05-20 | No | No | Historical |