Robaxin
- Product NDC
- 52244-449
- 11-digit product format
- 522440449
- Labeler code
- 52244
- Product ID
- 52244-449_53a60c30-a22d-42ce-8bca-761bb30f5b29
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Endo Pharmaceuticals Inc.
- Application
- NDA011011
- Marketing category
- NDA
- Marketing start
- 2011-08-18
- Marketing end
- 2021-03-31
- Substance
- METHOCARBAMOL
- Active strength
- 750 mg/1
- Pharmacologic classes
- Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 52244-449-10 | 52244044910 | 100 TABLET, FILM COATED in 1 BOTTLE (52244-449-10) | 2011-08-18 | 2021-03-31 | No | No | Current |