# Methocarbamol

NDC: 69584-612
Generic name: methocarbamol
Labeler / Manufacturer: Oxford Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190815

FDA application: ANDA040489

## Active ingredients

- METHOCARBAMOL: 750 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69584-612"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69584-612
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=06dc72a6-ef3a-425a-9194-a9d228093cc4