Molindone Hydrochloride (CorePharma, LLC)


Welcome to the PulseAid listing for the Molindone Hydrochloride drug offered from CorePharma, LLC. This Typical Antipsychotic [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: CorePharma, LLC
NON-PROPRIETARY NAME: Molindone Hydrochloride
SUBSTANCE NAME: MOLINDONE HYDROCHLORIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Typical Antipsychotic [EPC]
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2015-09-15
END MARKETING DATE: 2018-02-28


Molindone Hydrochloride HUMAN PRESCRIPTION DRUG Details:

Item DescriptionMolindone Hydrochloride from CorePharma, LLC
LABELER NAME: CorePharma, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 10(mg/1)
START MARKETING DATE: 2015-09-15
END MARKETING DATE: 2018-02-28
PRODUCT ID: 64720-229_587a6dc3-88ad-465e-9141-52ce5a9c1df8
PRODUCT NDC: 64720-229
APPLICATION NUMBER: ANDA090453

Other MOLINDONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
CorePharma, LLCMolindone Hydrochloride