# Methocarbamol Tablets, USP, 500 mg

NDC: 72789-499
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: 20240101

FDA application: ANDA212623

## 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:"72789-499"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-499
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6500c6eb-fa1e-46a5-839f-13047e107e97