Methocarbamol
- Product NDC
- 50090-0175
- 11-digit product format
- 500900175
- Labeler code
- 50090
- Product ID
- 50090-0175_a16cb586-4796-4f23-b8eb-c83f8871093f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040489
- Marketing category
- ANDA
- Marketing start
- 2003-01-29
- 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
- 2019-12-31
- 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 |
|---|
| 50090-0175-0 | Methocarbamol | 90 in 1 BOTTLE | TABLET | 90 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-0175 | METHOCARBAMOL TABLET [A-S MEDICATION SOLUTIONS] | 9 | Legacy NDC, 1 package rows | 20171222_d05f3784-f021-4e94-8ec1-a7b5036626ce.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50090-0175-0 | 50090017500 | 90 in 1 BOTTLE | Historical |