Methocarbamol
- Product NDC
- 35573-413
- 11-digit product format
- 355730413
- Labeler code
- 35573
- Product ID
- 35573-413_c3110908-1965-1576-e053-2995a90a524d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Burel Pharmaceuticals, Inc.
- Application
- ANDA209312
- Marketing category
- ANDA
- Marketing start
- 2019-09-30
- 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
- 2022-12-31
- 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 |
|---|
| 35573-413 | METHOCARBAMOL TABLET, COATED [BUREL PHARMACEUTICALS, INC.] | 7 | Legacy NDC | 20241023_81ecccd3-2eee-4b7e-832d-1acb44f779d5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35573-413-02 | 35573041302 | 100 TABLET, COATED in 1 BOTTLE (35573-413-02) | 2019-09-30 | 0000-00-00 | No | No | Current |
| 35573-413-04 | 35573041304 | 500 TABLET, COATED in 1 BOTTLE (35573-413-04) | 2019-09-30 | 0000-00-00 | No | No | Current |