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Calcitriol

NDC 70954-831 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA021068
Dosage form / routeSOLUTION · ORAL
Active ingredientsCALCITRIOL (1 ug/mL)
Marketing started20260513
Package count1

External sources

Source: openFDA. Public-domain (CC0).