FDA NDC Directory · JSON-LD · Markdown

Dantrolene Sodium

NDC 0115-4433 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076856
Dosage form / routeCAPSULE · ORAL
Active ingredientsDANTROLENE SODIUM (100 mg/1)
Marketing started20050301
Package count3

External sources

Source: openFDA. Public-domain (CC0).