# Methocarbamol

NDC: 85509-1770
Generic name: Methocarbamol Tablets
Labeler / Manufacturer: PHOENIX RX LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20180702

FDA application: ANDA209312

## 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:"85509-1770"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85509-1770
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=414b2fe0-fa2b-2b18-e063-6394a90ab2b9