Methocarbamol
- Product NDC
- 50090-5005
- 11-digit product format
- 500905005
- Labeler code
- 50090
- Product ID
- 50090-5005_1b2eb7b9-973a-4529-a906-3b6aa7df4994
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040489
- Marketing category
- ANDA
- Marketing start
- 2019-08-15
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5005-0 | 50090500500 | 42 TABLET in 1 BOTTLE (50090-5005-0) | 42 tablet | 2020-04-15 | 0000-00-00 | No | No | Current |
| 50090-5005-4 | 50090500504 | 7 TABLET in 1 BOTTLE (50090-5005-4) | 7 tablet | 2020-04-15 | 0000-00-00 | No | No | Current |