# Dantrolene

NDC: 0143-9297
Generic name: Dantrolene
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20170619

FDA application: ANDA204762

## Active ingredients

- DANTROLENE SODIUM: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9297"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9297
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ab0efc75-0598-4f4e-91ad-6195bb2661fe