# Meprobamate

NDC: 62332-020
Generic name: Meprobamate
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20160331

FDA application: ANDA090122

## Active ingredients

- MEPROBAMATE: 400 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62332-020"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-020
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3b255bcd-0218-44f8-830b-971f5ec45276