# Methocarbamol

NDC: 70518-4603
Generic name: Methocarbamol Tablets
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20260422

FDA application: ANDA209312

## 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:"70518-4603"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4603
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1dc3a5b1-c83b-406b-a59d-ce8075e4ccf9