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Quetiapine

NDC 68180-613 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204203
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsQUETIAPINE FUMARATE (150 mg/1)
Marketing started20170822
Package count1

External sources

Source: openFDA. Public-domain (CC0).