Methocarbamol
- Product NDC
- 71205-019
- 11-digit product format
- 712050019
- Labeler code
- 71205
- Product ID
- 71205-019_0c92dc46-6ade-4693-86da-7fa3411efff2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA200958
- Marketing category
- ANDA
- Marketing start
- 2015-07-13
- 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
- 2020-12-31
- 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 |
|---|
| 71205-019 | METHOCARBAMOL TABLET, FILM COATED [PROFICIENT RX LP] | 2 | Legacy NDC | 20191101_3dd098e2-7ae2-4245-a37c-05735f675e9d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-019-20 | 71205001920 | 20 TABLET, FILM COATED in 1 BOTTLE (71205-019-20) | 2018-04-02 | 0000-00-00 | No | No | Current |
| 71205-019-30 | 71205001930 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-019-30) | 2018-04-02 | 0000-00-00 | No | No | Current |
| 71205-019-40 | 71205001940 | 40 TABLET, FILM COATED in 1 BOTTLE (71205-019-40) | 2018-04-02 | 0000-00-00 | No | No | Current |
| 71205-019-45 | 71205001945 | 45 TABLET, FILM COATED in 1 BOTTLE (71205-019-45) | 2018-04-02 | 0000-00-00 | No | No | Current |
| 71205-019-60 | 71205001960 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-019-60) | 2018-04-02 | 0000-00-00 | No | No | Current |
| 71205-019-90 | 71205001990 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-019-90) | 2018-04-02 | 0000-00-00 | No | No | Current |