# Methocarbamol

NDC: 85509-1341
Generic name: Methocarbamol
Labeler / Manufacturer: PHOENIX RX LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200812

FDA application: ANDA213967

## Active ingredients

- METHOCARBAMOL: 750 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85509-1341"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85509-1341
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3b199152-bafc-e14a-e063-6394a90ab283