Diclofenac Potassium (NuCare Pharmaceuticals,Inc.)
Welcome to the PulseAid listing for the Diclofenac Potassium drug offered from NuCare Pharmaceuticals,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: | NuCare Pharmaceuticals,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: | 1999-09-17 |
| END MARKETING DATE: | 0000-00-00 |
Diclofenac Potassium HUMAN PRESCRIPTION DRUG Details:
| Item Description | Diclofenac Potassium from NuCare Pharmaceuticals,Inc. |
| LABELER NAME: | NuCare Pharmaceuticals,Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 50(mg/1) |
| START MARKETING DATE: | 1999-09-17 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 68071-4042_56692e8a-05da-5fd3-e054-00144ff88e88 |
| PRODUCT NDC: | 68071-4042 |
| APPLICATION NUMBER: | ANDA075463 |
Other DICLOFENAC POTASSIUM Pharmaceutical Manufacturers / Labelers:
