DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE (Lannett Company, Inc.)
Welcome to the PulseAid listing for the DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE drug offered from Lannett Company, Inc.. This Antidiarrheal [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic 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: | Lannett Company, Inc. |
| NON-PROPRIETARY NAME: | DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE |
| SUBSTANCE NAME: | DIPHENOXYLATE; ATROPINE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Antidiarrheal [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 1978-02-21 |
| END MARKETING DATE: | 0000-00-00 |
DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE HUMAN PRESCRIPTION DRUG Details:
| Item Description | DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE from Lannett Company, Inc. |
| LABELER NAME: | Lannett Company, Inc. |
| DEA SCHEDULE: | CV
|
| ACTIVE STRENGTH: | 2.5; .025(mg/1; mg/1) |
| START MARKETING DATE: | 1978-02-21 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0527-1170_f05da97e-88f0-489f-8008-193b604bf93b |
| PRODUCT NDC: | 0527-1170 |
| APPLICATION NUMBER: | ANDA085372 |
Other DIPHENOXYLATE; ATROPINE Pharmaceutical Manufacturers / Labelers:
