Methocarbamol
- Product NDC
- 70934-320
- 11-digit product format
- 709340320
- Labeler code
- 70934
- Product ID
- 70934-320_b7b1adaa-66e6-1424-e053-2995a90ac365
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA085159
- Marketing category
- ANDA
- Marketing start
- 2019-03-18
- Marketing end
- 0000-00-00
- Substance
- METHOCARBAMOL
- Active strength
- 750 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-320-20 | 70934032020 | 20 TABLET in 1 BOTTLE, PLASTIC (70934-320-20) | 20 tablet | 2019-03-18 | 0000-00-00 | No | No | Current |
| 70934-320-30 | 70934032030 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-320-30) | 30 tablet | 2019-05-23 | 0000-00-00 | No | No | Current |