DEXAMETHASONE SODIUM PHOSPHATE (Pfizer Laboratories Div Pfizer Inc)
Welcome to the PulseAid listing for the DEXAMETHASONE SODIUM PHOSPHATE drug offered from Pfizer Laboratories Div Pfizer Inc. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [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: | Pfizer Laboratories Div Pfizer Inc |
| NON-PROPRIETARY NAME: | DEXAMETHASONE SODIUM PHOSPHATE |
| SUBSTANCE NAME: | DEXAMETHASONE SODIUM PHOSPHATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| ROUTE: | INTRAMUSCULAR; INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2011-05-11 |
| END MARKETING DATE: | 0000-00-00 |
DEXAMETHASONE SODIUM PHOSPHATE HUMAN PRESCRIPTION DRUG Details:
| Item Description | DEXAMETHASONE SODIUM PHOSPHATE from Pfizer Laboratories Div Pfizer Inc |
| LABELER NAME: | Pfizer Laboratories Div Pfizer Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(mg/mL) |
| START MARKETING DATE: | 2011-05-11 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0069-4541_b66c70ec-f7b6-48d7-b7da-9268a368dd5d |
| PRODUCT NDC: | 0069-4541 |
| APPLICATION NUMBER: | ANDA040802 |
Other DEXAMETHASONE SODIUM PHOSPHATE Pharmaceutical Manufacturers / Labelers:
