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Fluorescein

NDC 70710-2045 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218651
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsFLUORESCEIN SODIUM (100 mg/mL)
Marketing started20260602
Package count1

External sources

Source: openFDA. Public-domain (CC0).