Methocarbamol
- Product NDC
- 42254-038
- 11-digit product format
- 422540038
- Labeler code
- 42254
- Product ID
- 42254-038_0defd325-d763-481e-afe8-86075e3c7e79
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA090200
- Marketing category
- ANDA
- Marketing start
- 2010-03-01
- 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
- 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 |
|---|
| 42254-038-07 | Methocarbamol | 07 in 1 BOTTLE | TABLET | 07 | | 1 |
| 42254-038-40 | Methocarbamol | 40 in 1 BOTTLE | TABLET | 40 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 42254-038 | METHOCARBAMOL TABLET [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 2 package rows | 20120411_0defd325-d763-481e-afe8-86075e3c7e79.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 42254-038-07 | 42254003807 | 07 in 1 BOTTLE | Historical |
| 42254-038-40 | 42254003840 | 40 in 1 BOTTLE | Historical |