HALOPERIDOL (Pfizer Laboratories Div Pfizer Inc)
Welcome to the PulseAid listing for the HALOPERIDOL drug offered from Pfizer Laboratories Div Pfizer 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: | Pfizer Laboratories Div Pfizer Inc |
| NON-PROPRIETARY NAME: | HALOPERIDOL LACTATE |
| SUBSTANCE NAME: | HALOPERIDOL LACTATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Typical Antipsychotic [EPC] |
| ROUTE: | INTRAMUSCULAR |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2011-05-10 |
| END MARKETING DATE: | 0000-00-00 |
HALOPERIDOL HUMAN PRESCRIPTION DRUG Details:
| Item Description | HALOPERIDOL from Pfizer Laboratories Div Pfizer Inc |
| LABELER NAME: | Pfizer Laboratories Div Pfizer Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5(mg/mL) |
| START MARKETING DATE: | 2011-05-10 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0069-0113_e0674bdd-1ce0-4c7b-a8ee-0983abb885f3 |
| PRODUCT NDC: | 0069-0113 |
| APPLICATION NUMBER: | ANDA078347 |
Other HALOPERIDOL LACTATE Pharmaceutical Manufacturers / Labelers:
