Methocarbamol
- Product NDC
- 69367-256
- 11-digit product format
- 693670256
- Labeler code
- 69367
- Product ID
- 69367-256_ae9df131-66a3-0ec7-e053-2995a90a02e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Application
- ANDA200958
- Marketing category
- ANDA
- Marketing start
- 2020-07-20
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69367-256 | METHOCARBAMOL TABLET, COATED [WESTMINSTER PHARMACEUTICALS, LLC] | 3 | Legacy NDC | 20240209_2199b810-fb84-4dac-b787-ade2b5f67e92.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69367-256-01 | 69367025601 | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-256-01) | 2020-07-20 | 0000-00-00 | No | No | Current |
| 69367-256-05 | 69367025605 | 500 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-256-05) | 2020-07-20 | 0000-00-00 | No | No | Current |