Methocarbamol
- Product NDC
- 69036-910
- 11-digit product format
- 690360910
- Labeler code
- 69036
- Product ID
- 69036-910_d56deff3-ec7d-49a0-9ad5-bbb109fc4de0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sallus Laboratories, LLC
- Application
- ANDA040489
- Marketing category
- ANDA
- Marketing start
- 2020-06-01
- Marketing end
- 0000-00-00
- Substance
- METHOCARBAMOL
- Active strength
- 500 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 69036-910-10 | 69036091010 | 100 TABLET in 1 BOTTLE (69036-910-10) | 100 tablet | 2020-06-01 | 0000-00-00 | No | No | Current |