# Methocarbamol Tablets, USP, 750 mg

NDC: 72789-521
Generic name: Methocarbamol
Labeler / Manufacturer: PD-Rx Pharmaceuticals, 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:"72789-521"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-521
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=60ebbdc4-7b0d-4ad4-a7ff-d99e9a1cb33c