Methocarbamol
- Product NDC
- 82982-038
- 11-digit product format
- 829820038
- Labeler code
- 82982
- Product ID
- 82982-038_198ccc85-82ff-0a2b-e063-6394a90a249f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Pharmasource Meds, LLC
- Application
- ANDA209312
- Marketing category
- ANDA
- Marketing start
- 2023-02-08
- Marketing end
- 2027-05-31
- Substance
- METHOCARBAMOL
- Active strength
- 750 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Methocarbamol
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METHOCARBAMOL | 750 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 125OD7737X |
| Rxcui | 197944 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82982-038-40 | Methocarbamol | 40 in 1 BOTTLE | TABLET, COATED | 40 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82982-038 | METHOCARBAMOL (METHOCARBAMOL TABLETS) TABLET, COATED [PHARMASOURCE MEDS, LLC] | 2 | Current NDC, 1 package rows | 20240602_f43a9389-c641-ce49-e053-2a95a90a537f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82982-038-40 | 82982003840 | 40 TABLET, COATED in 1 BOTTLE (82982-038-40) | 2023-02-08 | 2027-05-31 | No | No | Historical |