# Methocarbamol

NDC: 73352-510
Generic name: Methocarbamol
Labeler / Manufacturer: Trifluent Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20250210

FDA application: ANDA200958

## Active ingredients

- METHOCARBAMOL: 1000 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"73352-510"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=73352-510
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=de2e3af9-03ab-4dc8-b480-6866474ad1bd