Methocarbamol
- Product NDC
- 67046-538
- 11-digit product format
- 670460538
- Labeler code
- 67046
- Product ID
- 67046-538_a8f39d87-dcee-0079-e053-2995a90aefc7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA209312
- Marketing category
- ANDA
- Marketing start
- 2018-07-02
- 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
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 |
|---|
| 67046-538-30 | Methocarbamol | 30 in 1 BLISTER PACK | TABLET, COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-538 | METHOCARBAMOL (METHOCARBAMOL TABLETS) TABLET, COATED [CONTRACT PHARMACY SERVICES-PA] | 1 | Legacy NDC, 1 package rows | 20200626_a8f3b8c4-1d11-93c9-e053-2a95a90aa377.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67046-538-30 | 67046053830 | 30 TABLET, COATED in 1 BLISTER PACK (67046-538-30) | 2018-07-02 | 0000-00-00 | No | No | Current |