atomoxetine (Glenmark Pharmaceuticals Inc., USA)
Welcome to the PulseAid listing for the atomoxetine drug offered from Glenmark Pharmaceuticals Inc., USA. This Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [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: | Glenmark Pharmaceuticals Inc., USA |
| NON-PROPRIETARY NAME: | atomoxetine |
| SUBSTANCE NAME: | ATOMOXETINE HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Norepinephrine Reuptake Inhibitor [EPC],Norepinephrine Uptake Inhibitors [MoA] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2017-05-30 |
| END MARKETING DATE: | 0000-00-00 |
atomoxetine HUMAN PRESCRIPTION DRUG Details:
| Item Description | atomoxetine from Glenmark Pharmaceuticals Inc., USA |
| LABELER NAME: | Glenmark Pharmaceuticals Inc., USA |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(mg/1) |
| START MARKETING DATE: | 2017-05-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 68462-265_0ab8d905-e890-4e91-a730-3e5d12f5c23f |
| PRODUCT NDC: | 68462-265 |
| APPLICATION NUMBER: | ANDA079019 |
Other ATOMOXETINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
