Methocarbamol
- Product NDC
- 50090-0171
- 11-digit product format
- 500900171
- Labeler code
- 50090
- Product ID
- 50090-0171_1ab5f03a-d1ce-4e68-ba8b-e25c1505ebf0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 50090-0171-4 | Methocarbamol | 7 in 1 BOTTLE | TABLET | 7 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0171 | METHOCARBAMOL TABLET [A-S MEDICATION SOLUTIONS] | 8 | Legacy NDC, 1 package rows | 20190329_6abafef2-e988-4d37-a8ba-2263547af628.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 |
|---|
| 50090-0171-4 | 50090017104 | 7 TABLET in 1 BOTTLE (50090-0171-4) | 7 tablet | 2016-06-21 | 0000-00-00 | No | No | Current |