Methocarbamol
- Product NDC
- 43063-879
- 11-digit product format
- 430630879
- Labeler code
- 43063
- Product ID
- 43063-879_9b80b95f-2b4b-bcaf-e053-2995a90ad75a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA090200
- Marketing category
- ANDA
- Marketing start
- 2013-03-20
- 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 |
|---|
| 43063-879-20 | 43063087920 | 20 TABLET in 1 BOTTLE, PLASTIC (43063-879-20) | 20 tablet | 2018-09-20 | 0000-00-00 | No | No | Current |
| 43063-879-40 | 43063087940 | 40 TABLET in 1 BOTTLE, PLASTIC (43063-879-40) | 40 tablet | 2018-08-07 | 0000-00-00 | No | No | Current |