# Methocarbamol

NDC: 61919-616
Generic name: Methocarbamol
Labeler / Manufacturer: DIRECT RX
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20190418

FDA application: ANDA209312

## Active ingredients

- METHOCARBAMOL: 750 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"61919-616"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61919-616
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=31508051-c9cb-149b-e054-00144ff88e88