Methocarbamol
- Product NDC
- 0404-9909
- 11-digit product format
- 004049909
- Labeler code
- 0404
- Product ID
- 0404-9909_54db0c87-dfb0-4b00-a24d-e7f04c6507f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Henry Schein, Inc.
- Application
- ANDA204404
- Marketing category
- ANDA
- Marketing start
- 2022-01-13
- 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 |
|---|
| 0404-9909-10 | 00404990910 | 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9909-10) > 10 mL in 1 VIAL, SINGLE-DOSE | 2022-01-13 | 0000-00-00 | No | No | Current |