Daypro (G.D. Searle LLC Division of Pfizer Inc)
Welcome to the PulseAid listing for the Daypro drug offered from G.D. Searle LLC Division of Pfizer Inc. This Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [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: | G.D. Searle LLC Division of Pfizer Inc |
NON-PROPRIETARY NAME: | oxaprozin |
SUBSTANCE NAME: | OXAPROZIN |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1992-10-29 |
END MARKETING DATE: | 0000-00-00 |
Daypro HUMAN PRESCRIPTION DRUG Details:
Item Description | Daypro from G.D. Searle LLC Division of Pfizer Inc |
LABELER NAME: | G.D. Searle LLC Division of Pfizer Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 600(mg/1) |
START MARKETING DATE: | 1992-10-29 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0025-1381_fb232bdf-8642-4790-845a-e0bbd5c936eb |
PRODUCT NDC: | 0025-1381 |
APPLICATION NUMBER: | NDA018841 |
Other OXAPROZIN Pharmaceutical Manufacturers / Labelers: