PROCYSBIDelayed-release (Raptor Therapeutics Inc.)
Welcome to the PulseAid listing for the PROCYSBI drug offered from Raptor Therapeutics Inc.. This Cystine Depleting Agent [EPC],Cystine Disulfide Reduction [MoA] 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: | Raptor Therapeutics Inc. |
NON-PROPRIETARY NAME: | cysteamine bitartrate |
SUBSTANCE NAME: | CYSTEAMINE BITARTRATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Cystine Depleting Agent [EPC],Cystine Disulfide Reduction [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | CAPSULE, DELAYED RELEASE PELLETS |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2013-04-30 |
END MARKETING DATE: | 0000-00-00 |
PROCYSBI Delayed-release HUMAN PRESCRIPTION DRUG Details:
Item Description | PROCYSBI Delayed-release from Raptor Therapeutics Inc. |
LABELER NAME: | Raptor Therapeutics Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 25(mg/1) |
START MARKETING DATE: | 2013-04-30 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 49663-001_3c71b268-ffe6-4693-b2eb-162f4852970a |
PRODUCT NDC: | 49663-001 |
APPLICATION NUMBER: | NDA203389 |
Other CYSTEAMINE BITARTRATE Pharmaceutical Manufacturers / Labelers: