Haloperidol (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Haloperidol drug offered from Teva Pharmaceuticals USA, Inc.. This Typical Antipsychotic [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: | Teva Pharmaceuticals USA, Inc. |
| NON-PROPRIETARY NAME: | Haloperidol lactate |
| SUBSTANCE NAME: | HALOPERIDOL LACTATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Typical Antipsychotic [EPC] |
| ROUTE: | ORAL |
| DOSAGE FORM: | SOLUTION, CONCENTRATE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 1988-12-01 |
| END MARKETING DATE: | 0000-00-00 |
Haloperidol HUMAN PRESCRIPTION DRUG Details:
| Item Description | Haloperidol from Teva Pharmaceuticals USA, Inc. |
| LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 2(mg/mL) |
| START MARKETING DATE: | 1988-12-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0093-9604_fcdcb3a6-0042-4b97-82e1-b32a94b98575 |
| PRODUCT NDC: | 0093-9604 |
| APPLICATION NUMBER: | ANDA071617 |
Other HALOPERIDOL LACTATE Pharmaceutical Manufacturers / Labelers:
