Methocarbamol
- Product NDC
- 70934-231
- 11-digit product format
- 709340231
- Labeler code
- 70934
- Product ID
- 70934-231_b7c398c7-1742-0937-e053-2995a90a3f9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA208507
- Marketing category
- ANDA
- Marketing start
- 2019-01-15
- Marketing end
- 0000-00-00
- Substance
- METHOCARBAMOL
- Active strength
- 500 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-231-14 | 70934023114 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-231-14) | 2019-01-15 | 0000-00-00 | No | No | Current |