Cuprimine (Aton Pharma, Inc.)


Welcome to the PulseAid listing for the Cuprimine drug offered from Aton Pharma, Inc.. This Antirheumatic Agent [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: Aton Pharma, Inc.
NON-PROPRIETARY NAME: Penicillamine
SUBSTANCE NAME: PENICILLAMINE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Antirheumatic Agent [EPC]
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1970-12-04
END MARKETING DATE: 0000-00-00


Cuprimine HUMAN PRESCRIPTION DRUG Details:

Item DescriptionCuprimine from Aton Pharma, Inc.
LABELER NAME: Aton Pharma, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 250(mg/1)
START MARKETING DATE: 1970-12-04
END MARKETING DATE: 0000-00-00
PRODUCT ID: 25010-705_ab9e4ced-8667-4755-8af9-41597daa082c
PRODUCT NDC: 25010-705
APPLICATION NUMBER: NDA019853

Other PENICILLAMINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Aton Pharma, Inc.Cuprimine
Meda Pharmaceuticals Inc.Depen