Prochlorperazine Edisylate (Baxter Healthcare Corporation)
Welcome to the PulseAid listing for the Prochlorperazine Edisylate drug offered from Baxter Healthcare Corporation. This Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] 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: | Baxter Healthcare Corporation |
| NON-PROPRIETARY NAME: | Prochlorperazine Edisylate |
| SUBSTANCE NAME: | PROCHLORPERAZINE EDISYLATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
| ROUTE: | INTRAMUSCULAR; INTRAVENOUS |
| DOSAGE FORM: | INJECTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2011-01-14 |
| END MARKETING DATE: | 0000-00-00 |
Prochlorperazine Edisylate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Prochlorperazine Edisylate from Baxter Healthcare Corporation |
| LABELER NAME: | Baxter Healthcare Corporation |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 5(mg/mL) |
| START MARKETING DATE: | 2011-01-14 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0641-0491_7b251584-d98e-459b-9a71-8574bd5733d1 |
| PRODUCT NDC: | 0641-0491 |
| APPLICATION NUMBER: | ANDA089903 |
Other PROCHLORPERAZINE EDISYLATE Pharmaceutical Manufacturers / Labelers:
