Methocarbamol
- Product NDC
- 70860-653
- 11-digit product format
- 708600653
- Labeler code
- 70860
- Product ID
- 70860-653_ac0ddbd6-7bbc-48aa-b312-95db819b0a04
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Athenex Pharmaceutical Division, LLC.
- Application
- ANDA211504
- Marketing category
- ANDA
- Marketing start
- 2018-11-30
- 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
- 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 |
|---|
| 70860-653-10 | 70860065310 | 25 VIAL in 1 CARTON (70860-653-10) > 10 mL in 1 VIAL (70860-653-41) | 25 vial | 2018-11-30 | 0000-00-00 | No | No | Current |