Methocarbamol
- Product NDC
- 50090-4162
- 11-digit product format
- 500904162
- Labeler code
- 50090
- Product ID
- 50090-4162_b1640d97-ea3d-4948-a3ef-968935c1a92e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA208507
- Marketing category
- ANDA
- Marketing start
- 2018-01-15
- Marketing end
- 0000-00-00
- Substance
- METHOCARBAMOL
- Active strength
- 750 mg/1
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4162-0 | 50090416200 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-4162-0) | 2019-02-26 | 0000-00-00 | No | No | Current |