Methocarbamol
- Product NDC
- 50090-4164
- 11-digit product format
- 500904164
- Labeler code
- 50090
- Product ID
- 50090-4164_113f5965-41c8-4d0e-b470-25cf61147a37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4164-0 | 50090416400 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-4164-0) | 2019-02-26 | 0000-00-00 | No | No | Current |
| 50090-4164-1 | 50090416401 | 40 TABLET, FILM COATED in 1 BOTTLE (50090-4164-1) | 2019-06-12 | 0000-00-00 | No | No | Current |
| 50090-4164-2 | 50090416402 | 28 TABLET, FILM COATED in 1 BOTTLE (50090-4164-2) | 2019-06-12 | 0000-00-00 | No | No | Current |
| 50090-4164-3 | 50090416403 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-4164-3) | 2019-06-12 | 0000-00-00 | No | No | Current |
| 50090-4164-4 | 50090416404 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-4164-4) | 2019-06-12 | 0000-00-00 | No | No | Current |
| 50090-4164-6 | 50090416406 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-4164-6) | 2019-06-12 | 0000-00-00 | No | No | Current |
| 50090-4164-7 | 50090416407 | 12 TABLET, FILM COATED in 1 BOTTLE (50090-4164-7) | 2019-06-12 | 0000-00-00 | No | No | Current |