Methocarbamol
- Product NDC
- 0179-0092
- 11-digit product format
- 001790092
- Labeler code
- 0179
- Product ID
- 0179-0092_7bc2989f-df9f-e8af-e053-2991aa0a0bf2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methocarbamol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA090200
- Marketing category
- ANDA
- Marketing start
- 2011-06-06
- Marketing end
- 2020-01-31
- Substance
- METHOCARBAMOL
- Active strength
- 500 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