# Methocarbamol Tablets, USP, 750 mg

NDC: 63561-0174
Generic name: Methocarbamol
Labeler / Manufacturer: Granulation Technology, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250610

FDA application: ANDA212623

## 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:"63561-0174"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63561-0174
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=70c5342c-9597-4fe6-863c-f8ae4adc063a