Zithromax (Pfizer Laboratories Div Pfizer Inc)
Welcome to the PulseAid listing for the Zithromax drug offered from Pfizer Laboratories Div Pfizer Inc. This Macrolide Antimicrobial [EPC],Macrolides [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: | Pfizer Laboratories Div Pfizer Inc |
| NON-PROPRIETARY NAME: | azithromycin dihydrate |
| SUBSTANCE NAME: | AZITHROMYCIN DIHYDRATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 1997-01-30 |
| END MARKETING DATE: | 0000-00-00 |
Zithromax HUMAN PRESCRIPTION DRUG Details:
| Item Description | Zithromax from Pfizer Laboratories Div Pfizer Inc |
| LABELER NAME: | Pfizer Laboratories Div Pfizer Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 500(mg/5mL) |
| START MARKETING DATE: | 1997-01-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0069-0400_7405ed29-0b54-4f78-9fd6-18c03a0d255d |
| PRODUCT NDC: | 0069-0400 |
| APPLICATION NUMBER: | NDA050733 |
Other AZITHROMYCIN DIHYDRATE Pharmaceutical Manufacturers / Labelers:
