Methocarbamol
- Product NDC
- 70518-3096
- 11-digit product format
- 705183096
- Labeler code
- 70518
- Product ID
- 70518-3096_ceb46d21-68be-bd34-e053-2a95a90acb1d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040489
- Marketing category
- ANDA
- Marketing start
- 2021-05-18
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3096 | METHOCARBAMOL TABLET [REMEDYREPACK INC.] | 8 | Legacy NDC | 20250104_3b91fc6f-d9c6-45b2-a5ca-0f890b8d0d91.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3096-0 | 70518309600 | 30 TABLET in 1 BLISTER PACK (70518-3096-0) | 30 tablet | 2021-05-18 | 0000-00-00 | No | No | Current |
| 70518-3096-1 | 70518309601 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-3096-1) | 90 tablet | 2021-05-26 | 0000-00-00 | No | No | Current |
| 70518-3096-2 | 70518309602 | 60 TABLET in 1 BOTTLE, PLASTIC (70518-3096-2) | 60 tablet | 2021-08-30 | 0000-00-00 | No | No | Current |
| 70518-3096-3 | 70518309603 | 20 TABLET in 1 BOTTLE, PLASTIC (70518-3096-3) | 20 tablet | 2021-10-15 | 0000-00-00 | No | No | Current |