# Methocarbamol

NDC: 68788-8172
Generic name: Methocarbamol Tablets
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20220425

FDA application: ANDA209312

## Active ingredients

- METHOCARBAMOL: 750 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8172"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8172
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=43f83b87-e169-46fe-98bd-6af373595bd3