Methocarbamol
- Product NDC
- 52584-073
- 11-digit product format
- 525840073
- Labeler code
- 52584
- Product ID
- 52584-073_075e75d9-14d9-4577-9f2f-7d2fb71c9ae9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA204404
- Marketing category
- ANDA
- Marketing start
- 2018-09-28
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-073-00 | 52584007300 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-073-00) > 10 mL in 1 VIAL, SINGLE-DOSE | 2018-09-28 | 0000-00-00 | No | No | Current |