FDA NDC Directory · JSON-LD · Markdown

dantrolene sodium

NDC 70518-4668 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryNDA AUTHORIZED GENERIC · App NDA017443
Dosage form / routeCAPSULE · ORAL
Active ingredientsDANTROLENE SODIUM (50 mg/1)
Marketing started20260527
Package count1

External sources

Source: openFDA. Public-domain (CC0).