Methocarbamol
- Product NDC
- 70518-2131
- 11-digit product format
- 705182131
- Labeler code
- 70518
- Product ID
- 70518-2131_c6259789-438d-211a-e053-2995a90aa5c4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA208507
- Marketing category
- ANDA
- Marketing start
- 2019-06-05
- 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
- 2022-12-31
- 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 |
|---|
| 70518-2131-0 | 70518213100 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2131-0) | 2019-06-05 | 0000-00-00 | No | No | Current |