Methocarbamol
- Product NDC
- 50090-0178
- 11-digit product format
- 500900178
- Labeler code
- 50090
- Product ID
- 50090-0178_5e95473b-4d46-42f7-8f92-02c597b0f864
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA085159
- Marketing category
- ANDA
- Marketing start
- 2000-01-01
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0178-0 | 50090017800 | 40 TABLET in 1 BOTTLE (50090-0178-0) | 40 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |