Methocarbamol
- Product NDC
- 67296-0711
- 11-digit product format
- 672960711
- Labeler code
- 67296
- Product ID
- 67296-0711_9c9ae05a-bccc-79b6-e053-2a95a90a88ca
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- 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
- 2021-12-31
- 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 |
|---|
| 67296-0711-1 | Methocarbamol | 30 in 1 BOTTLE | TABLET | 30 | | 4 |
| 67296-0711-2 | Methocarbamol | 15 in 1 BOTTLE | TABLET | 15 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0711 | METHOCARBAMOL TABLET [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 2 package rows | 20200123_416084e3-c5ab-17c2-e054-00144ff8d46c.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 |
|---|
| 67296-0711-1 | 67296071101 | 30 TABLET in 1 BOTTLE (67296-0711-1) | 30 tablet | 2003-01-29 | 0000-00-00 | No | No | Current |
| 67296-0711-2 | 67296071102 | 15 TABLET in 1 BOTTLE (67296-0711-2) | 15 tablet | 2003-01-29 | 0000-00-00 | No | No | Current |