Methocarbamol
- Product NDC
- 50090-1782
- 11-digit product format
- 500901782
- Labeler code
- 50090
- Product ID
- 50090-1782_7b8f32cc-d3af-4bbd-b49b-50ab6d0c4559
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090200
- Marketing category
- ANDA
- Marketing start
- 2013-03-20
- 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
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 |
|---|
| 50090-1782-4 | Methocarbamol | 7 in 1 BOTTLE | TABLET | 7 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-1782 | METHOCARBAMOL TABLET [A-S MEDICATION SOLUTIONS] | 7 | Legacy NDC, 1 package rows | 20210617_82d61d90-dd98-4fbd-8bdf-77fed14be30e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1782-4 | 50090178204 | 7 TABLET in 1 BOTTLE (50090-1782-4) | 7 tablet | 2015-04-16 | 0000-00-00 | No | No | Current |