Donnatal (PD-Rx Pharmaceuticals, Inc.)
Welcome to the PulseAid listing for the Donnatal drug offered from PD-Rx Pharmaceuticals, Inc.. This Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [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: | PD-Rx Pharmaceuticals, Inc. |
NON-PROPRIETARY NAME: | PHENOBARBITAL, HYOSCYAMINE SULFATE, ATROPINE SULFATE, SCOPOLAMINE HYDROBROMIDE |
SUBSTANCE NAME: | PHENOBARBITAL; HYOSCYAMINE SULFATE; ATROPINE SULFATE; SCOPOLAMINE HYDROBROMIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 2008-05-07 |
END MARKETING DATE: | 0000-00-00 |
Donnatal HUMAN PRESCRIPTION DRUG Details:
Item Description | Donnatal from PD-Rx Pharmaceuticals, Inc. |
LABELER NAME: | PD-Rx Pharmaceuticals, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 16.2; .1037; .0194; .0065(mg/1; mg/1; mg/1; mg/1) |
START MARKETING DATE: | 2008-05-07 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 43063-601_5c3a89ef-a0c9-bb12-e053-2a91aa0aeb0b |
PRODUCT NDC: | 43063-601 |
APPLICATION NUMBER: | |
Other PHENOBARBITAL; HYOSCYAMINE SULFATE; ATROPINE SULFATE; SCOPOLAMINE HYDROBROMIDE Pharmaceutical Manufacturers / Labelers: