Methocarbamol
- Product NDC
- 71610-134
- 11-digit product format
- 716100134
- Labeler code
- 71610
- Product ID
- 71610-134_299592bc-464b-4a36-8ece-fee27da7db8c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA209312
- Marketing category
- ANDA
- Marketing start
- 2018-07-02
- 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 |
|---|
| 71610-134-53 | 71610013453 | 60 TABLET, COATED in 1 BOTTLE (71610-134-53) | 2018-08-27 | No | No | Historical |
| 71610-134-60 | 71610013460 | 90 TABLET, COATED in 1 BOTTLE (71610-134-60) | 2018-08-27 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Methocarbamol Tablets Rx Only | Aphena Pharma Solutions - Tennessee, LLC | 2018-09-12 | HUMAN PRESCRIPTION DRUG LABEL | 1 |