Methocarbamol
- Product NDC
- 55700-218
- 11-digit product format
- 557000218
- Labeler code
- 55700
- Product ID
- 55700-218_7099f07d-27b6-4803-8c37-c0f91238aa15
- 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
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-218-30 | 55700021830 | 30 TABLET in 1 BOTTLE (55700-218-30) | 30 tablet | 2021-11-26 | 0000-00-00 | No | No | Current |
| 55700-218-60 | 55700021860 | 60 TABLET in 1 BOTTLE (55700-218-60) | 60 tablet | 2021-11-26 | 0000-00-00 | No | No | Current |
| 55700-218-90 | 55700021890 | 90 TABLET in 1 BOTTLE (55700-218-90) | 90 tablet | 2021-11-26 | 0000-00-00 | No | No | Current |