Atomoxetine hydrochloride (Sandoz Inc)
Welcome to the PulseAid listing for the Atomoxetine hydrochloride drug offered from Sandoz Inc. 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: | Sandoz Inc |
| NON-PROPRIETARY NAME: | Atomoxetine hydrochloride |
| 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: | 2010-12-15 |
| END MARKETING DATE: | 0000-00-00 |
Atomoxetine hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Atomoxetine hydrochloride from Sandoz Inc |
| LABELER NAME: | Sandoz Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(mg/1) |
| START MARKETING DATE: | 2010-12-15 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0781-2260_6b194d5b-7326-4baf-9e5a-d9ada2f369ca |
| PRODUCT NDC: | 0781-2260 |
| APPLICATION NUMBER: | ANDA079018 |
Other ATOMOXETINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
