Methocarbamol
- Product NDC
- 50090-4309
- 11-digit product format
- 500904309
- Labeler code
- 50090
- Product ID
- 50090-4309_d99bc466-2182-4144-9ec0-a67e0988a463
- 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
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 125OD7737X | METHOCARBAMOL | 532-03-6 | METHOCARBAMOL |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4309-0 | 50090430900 | 10 TABLET, FILM COATED in 1 BOTTLE (50090-4309-0) | 2019-09-18 | 0000-00-00 | No | No | Current |
| 50090-4309-2 | 50090430902 | 7 TABLET, FILM COATED in 1 BOTTLE (50090-4309-2) | 2019-05-28 | 0000-00-00 | No | No | Current |
| 50090-4309-4 | 50090430904 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-4309-4) | 2019-05-31 | 0000-00-00 | No | No | Current |