Methocarbamol
- Product NDC
- 67296-1825
- 11-digit product format
- 672961825
- Labeler code
- 67296
- Product ID
- 67296-1825_d61eee18-c0b9-6627-e053-2995a90af89e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA208507
- Marketing category
- ANDA
- Marketing start
- 2018-01-15
- 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
- 2023-12-31
- 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 |
|---|
| 67296-1825-3 | Methocarbamol | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1825 | METHOCARBAMOL TABLET, FILM COATED [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 1 package rows | 20240719_b1a840cf-47a9-b931-e053-2a95a90a1047.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 |
|---|
| 67296-1825-3 | 67296182503 | 30 TABLET, FILM COATED in 1 BOTTLE (67296-1825-3) | 2018-01-15 | 0000-00-00 | No | No | Current |