Methocarbamol
- Product NDC
- 35356-887
- 11-digit product format
- 353560887
- Labeler code
- 35356
- Product ID
- 35356-887_430726de-472b-4895-9ee4-edc5430600bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products LLC
- Application
- ANDA090200
- Marketing category
- ANDA
- Marketing start
- 2013-03-20
- 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
- 2023-12-31
- 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 |
|---|
| 35356-887-30 | 35356088730 | 30 TABLET in 1 BOTTLE (35356-887-30) | 30 tablet | 2021-11-26 | 0000-00-00 | No | No | Current |
| 35356-887-60 | 35356088760 | 60 TABLET in 1 BOTTLE (35356-887-60) | 60 tablet | 2013-03-20 | 0000-00-00 | No | No | Current |
| 35356-887-90 | 35356088790 | 90 TABLET in 1 BOTTLE (35356-887-90) | 90 tablet | 2013-03-20 | 0000-00-00 | No | No | Current |