MEPROBAMATE 200 mg/1
MEPROBAMATE · TABLET · Alembic Pharmaceuticals Limited
No Recall History
Plain English
MEPROBAMATE is a tablet containing meprobamate at 200 mg/1, taken oral. Manufactured by Alembic Pharmaceuticals Limited.
Key Facts
- Brand Name
- MEPROBAMATE
- Generic Name
- MEPROBAMATE
- NDC Code (Product)
46708-019- Manufacturer
- Alembic Pharmaceuticals Limited
- Strength
- 200 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule IV (Controlled)
- Application #
- ANDA090122
- Marketing Start
- 07/23/2013
Recall History
No Recall HistoryFrequently Asked Questions
What is MEPROBAMATE used for?
MEPROBAMATE contains MEPROBAMATE. It is a tablet taken oral. Consult your doctor for specific uses.
Is MEPROBAMATE a controlled substance?
Yes, MEPROBAMATE is classified as CIV under the DEA Controlled Substances Act.
What is the generic name for MEPROBAMATE?
The generic name for MEPROBAMATE is MEPROBAMATE. There are 4 other brand versions of MEPROBAMATE.
What is the NDC code for MEPROBAMATE 200 mg/1?
The NDC (National Drug Code) for MEPROBAMATE 200 mg/1 is 46708-019, listed by Alembic Pharmaceuticals Limited.