Methocarbamol
- Product NDC
- 50436-0533
- 11-digit product format
- 504360533
- Labeler code
- 50436
- Product ID
- 50436-0533_731fdb81-63d9-4aa9-a87e-e7123fdabbc1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA090200
- Marketing category
- ANDA
- Marketing start
- 2013-03-20
- 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
- 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 |
|---|
| 50436-0533-1 | Methocarbamol | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
| 50436-0533-2 | Methocarbamol | 60 in 1 BOTTLE | TABLET | 60 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0533 | METHOCARBAMOL TABLET [UNIT DOSE SERVICES] | 4 | Legacy NDC, 2 package rows | 20171012_c54e8984-3655-4f09-ac2f-e6ea4c394121.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0533-1 | 50436053301 | 30 in 1 BOTTLE | Historical |
| 50436-0533-2 | 50436053302 | 60 in 1 BOTTLE | Historical |