Diclofenac Potassium (Sandoz Inc)
Welcome to the PulseAid listing for the Diclofenac Potassium drug offered from Sandoz Inc. This Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],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: | Sandoz Inc |
NON-PROPRIETARY NAME: | Diclofenac Potassium |
SUBSTANCE NAME: | DICLOFENAC POTASSIUM |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 1998-11-20 |
END MARKETING DATE: | 0000-00-00 |
Diclofenac Potassium HUMAN PRESCRIPTION DRUG Details:
Item Description | Diclofenac Potassium from Sandoz Inc |
LABELER NAME: | Sandoz Inc |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 50(mg/1) |
START MARKETING DATE: | 1998-11-20 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0781-5017_731f86ee-7751-4dfb-aad6-b367385f3397 |
PRODUCT NDC: | 0781-5017 |
APPLICATION NUMBER: | ANDA075229 |
Other DICLOFENAC POTASSIUM Pharmaceutical Manufacturers / Labelers: