# Methocarbamol

NDC: 70868-901
Generic name: methocarbamol
Labeler / Manufacturer: Key Therapeutics
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20191226

FDA application: ANDA040489

## 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:"70868-901"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70868-901
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a88a6c84-b55a-4b6b-ac01-554079f6e304