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Thioridazine Hydrochloride

NDC 0378-0618 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namethioridazine hydrochloride
Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA088004
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTHIORIDAZINE HYDROCHLORIDE (100 mg/1)
Marketing started19831118
Package count1

External sources

Source: openFDA. Public-domain (CC0).