METHADONE HYDROCHLORIDE (PD-Rx Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the METHADONE HYDROCHLORIDE drug offered from PD-Rx Pharmaceuticals, Inc.. This Full Opioid Agonists [MoA],Opioid Agonist [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: | PD-Rx Pharmaceuticals, Inc. |
NON-PROPRIETARY NAME: | METHADONE HYDROCHLORIDE |
SUBSTANCE NAME: | METHADONE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1947-08-13 |
END MARKETING DATE: | 0000-00-00 |
METHADONE HYDROCHLORIDE HUMAN PRESCRIPTION DRUG Details:
Item Description | METHADONE HYDROCHLORIDE from PD-Rx Pharmaceuticals, Inc. |
LABELER NAME: | PD-Rx Pharmaceuticals, Inc. |
DEA SCHEDULE: | CII
|
ACTIVE STRENGTH: | 5(mg/1) |
START MARKETING DATE: | 1947-08-13 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 43063-222_5796a492-88a1-9a53-e053-2a91aa0a8e96 |
PRODUCT NDC: | 43063-222 |
APPLICATION NUMBER: | NDA006134 |
Other METHADONE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: