Methocarbamol
- Product NDC
- 63629-4422
- 11-digit product format
- 636294422
- Labeler code
- 63629
- Product ID
- 63629-4422_2a688115-8e10-4313-8598-821b523af21d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040489
- Marketing category
- ANDA
- Marketing start
- 2003-01-29
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#