CORGARD (Pfizer Laboratories Div Pfizer Inc)
Welcome to the PulseAid listing for the CORGARD drug offered from Pfizer Laboratories Div Pfizer Inc. This Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [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: | Pfizer Laboratories Div Pfizer Inc |
NON-PROPRIETARY NAME: | nadolol |
SUBSTANCE NAME: | NADOLOL |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1979-12-10 |
END MARKETING DATE: | 0000-00-00 |
CORGARD HUMAN PRESCRIPTION DRUG Details:
Item Description | CORGARD from Pfizer Laboratories Div Pfizer Inc |
LABELER NAME: | Pfizer Laboratories Div Pfizer Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 20(mg/1) |
START MARKETING DATE: | 1979-12-10 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 60793-800_15c2b40b-81b9-404a-9d49-b30498c8d3ef |
PRODUCT NDC: | 60793-800 |
APPLICATION NUMBER: | NDA018063 |
Other NADOLOL Pharmaceutical Manufacturers / Labelers: