# dantrolene sodium

NDC: 70518-4668
Generic name: dantrolene sodium
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: NDA AUTHORIZED GENERIC
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20260527

FDA application: NDA017443

## Active ingredients

- DANTROLENE SODIUM: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4668"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4668