# Methocarbamol

NDC: 87063-040
Generic name: Methocarbamol
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230209

FDA application: ANDA213967

## Active ingredients

- METHOCARBAMOL: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"87063-040"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=87063-040
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7f297ac6-a580-4539-a770-fe5d15c2b922