Methocarbamol
- Product NDC
- 0517-1825
- 11-digit product format
- 005171825
- Labeler code
- 0517
- Product ID
- 0517-1825_d43f74d6-5d9d-493a-9c21-ec10c53ceebf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- American Regent, Inc.
- Application
- ANDA207496
- Marketing category
- ANDA
- Marketing start
- 2018-01-15
- Marketing end
- 0000-00-00
- Substance
- METHOCARBAMOL
- Active strength
- 100 mg/mL
- 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
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0517-1825-10 | 00517182510 | 10 VIAL in 1 CARTON (0517-1825-10) > 10 mL in 1 VIAL (0517-1825-01) | 10 vial | 2018-01-15 | 0000-00-00 | No | No | Current |