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Quetiapine

NDC 71205-401 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA202152
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsQUETIAPINE FUMARATE (200 mg/1)
Marketing started20120328
Package count3

External sources

Source: openFDA. Public-domain (CC0).