Methocarbamol
- Product NDC
- 70868-910
- 11-digit product format
- 708680910
- Labeler code
- 70868
- Product ID
- 70868-910_24143189-700c-75f8-e063-6394a90ac5ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Key Therapeutics
- Application
- ANDA040489
- Marketing category
- ANDA
- Marketing start
- 2021-01-01
- Substance
- METHOCARBAMOL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Methocarbamol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METHOCARBAMOL | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 125OD7737X |
| Rxcui | 197943 |
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 |
|---|
| 70868-910-10 | Methocarbamol | 100 in 1 BOTTLE | TABLET | 100 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70868-910 | METHOCARBAMOL TABLET [KEY THERAPEUTICS] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241019_cf931001-95bd-4900-98d5-f5ef54b49d99.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 |
|---|
| 70868-910-10 | 70868091010 | 100 TABLET in 1 BOTTLE (70868-910-10) | 100 tablet | 2021-01-01 | 0000-00-00 | No | No | Current |