FDA NDC Directory · JSON-LD · Markdown

FLUORESCEIN

NDC 83854-048 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic namefluorescein
Labeler / ManufacturerAnthea Pharma Private Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218651
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsFLUORESCEIN SODIUM (100 mg/mL)
Marketing started20261014
Package count1

External sources

Source: openFDA. Public-domain (CC0).