# Dantrolene Sodium

NDC: 0115-4433
Generic name: Dantrolene Sodium
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20050301

FDA application: ANDA076856

## Active ingredients

- DANTROLENE SODIUM: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0115-4433"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0115-4433
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c3c45b27-f786-456e-95d6-2e38ef36190a