FDA NDC Directory · JSON-LD · Markdown

Bumetanide

NDC 83854-007 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerAnthea Pharma Private Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA220427
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsBUMETANIDE (.25 mg/mL)
Marketing started20260227
Package count1

External sources

Source: openFDA. Public-domain (CC0).