Methocarbamol
- Product NDC
- 68788-7809
- 11-digit product format
- 687887809
- Labeler code
- 68788
- Product ID
- 68788-7809_7eef3524-07ab-4cce-a901-b7b789035da1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA208507
- Marketing category
- ANDA
- Marketing start
- 2018-01-15
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7809-1 | 68788780901 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7809-1) | 2020-10-29 | 0000-00-00 | No | No | Current |
| 68788-7809-2 | 68788780902 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-7809-2) | 2020-10-29 | 0000-00-00 | No | No | Current |
| 68788-7809-3 | 68788780903 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7809-3) | 2020-10-29 | 0000-00-00 | No | No | Current |
| 68788-7809-6 | 68788780906 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7809-6) | 2020-10-29 | 0000-00-00 | No | No | Current |
| 68788-7809-8 | 68788780908 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-7809-8) | 2020-10-29 | 0000-00-00 | No | No | Current |
| 68788-7809-9 | 68788780909 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7809-9) | 2020-10-29 | 0000-00-00 | No | No | Current |