Methocarbamol
- Product NDC
- 68475-002
- 11-digit product format
- 684750002
- Labeler code
- 68475
- Product ID
- 68475-002_18f370d8-7ea7-4595-bcdf-ad0b80a1c193
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Navinta LLC
- Application
- ANDA206071
- Marketing category
- ANDA
- Marketing start
- 2020-12-22
- 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
- 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 |
|---|
| 68475-002-25 | 68475000225 | 25 VIAL in 1 CARTON (68475-002-25) > 10 mL in 1 VIAL (68475-002-10) | 25 vial | 2020-12-22 | 0000-00-00 | No | No | Current |