Haloperidol (Breckenridge Pharmaceutical, Inc.)
Welcome to the PulseAid listing for the Haloperidol drug offered from Breckenridge Pharmaceutical, 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: | Breckenridge Pharmaceutical, Inc. |
| NON-PROPRIETARY NAME: | Haloperidol Lactate |
| SUBSTANCE NAME: | HALOPERIDOL LACTATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Typical Antipsychotic [EPC] |
| ROUTE: | INTRAMUSCULAR |
| DOSAGE FORM: | INJECTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-01-04 |
| END MARKETING DATE: | 0000-00-00 |
Haloperidol HUMAN PRESCRIPTION DRUG Details:
| Item Description | Haloperidol from Breckenridge Pharmaceutical, Inc. |
| LABELER NAME: | Breckenridge Pharmaceutical, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5(mg/mL) |
| START MARKETING DATE: | 2016-01-04 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51991-933_f898eb58-8608-4c9e-aad3-78c1da2c7b41 |
| PRODUCT NDC: | 51991-933 |
| APPLICATION NUMBER: | ANDA076774 |
Other HALOPERIDOL LACTATE Pharmaceutical Manufacturers / Labelers:
