ZMAX (Pfizer Laboratories Div Pfizer Inc)
Welcome to the PulseAid listing for the ZMAX 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: | ORAL |
DOSAGE FORM: | POWDER, FOR SUSPENSION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1995-06-10 |
END MARKETING DATE: | 0000-00-00 |
ZMAX HUMAN PRESCRIPTION DRUG Details:
Item Description | ZMAX from Pfizer Laboratories Div Pfizer Inc |
LABELER NAME: | Pfizer Laboratories Div Pfizer Inc |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 2(g/60mL) |
START MARKETING DATE: | 1995-06-10 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0069-4170_4f1c85cd-1e0e-4ca8-8590-fb4ce83e9b53 |
PRODUCT NDC: | 0069-4170 |
APPLICATION NUMBER: | NDA050797 |
Other AZITHROMYCIN DIHYDRATE Pharmaceutical Manufacturers / Labelers: