Methocarbamol
- Product NDC
- 67046-466
- 11-digit product format
- 670460466
- Labeler code
- 67046
- Product ID
- 67046-466_09721fb9-d3bd-4fc3-be79-79bc653a8289
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA085159
- Marketing category
- ANDA
- Marketing start
- 2000-01-01
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67046-466-30 | Methocarbamol | 30 in 1 BLISTER PACK | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-466 | METHOCARBAMOL TABLET [CONTRACT PHARMACY SERVICES-PA] | 2 | Legacy NDC, 1 package rows | 20100824_b86839dd-e0fc-4319-9abc-bcf69cf7a6e2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67046-466-30 | 67046046630 | 30 in 1 BLISTER PACK | Historical |