| NDC Code | 55289-781-21 |
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| Package Description | 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-781-21) |
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| Product NDC | 55289-781 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Diclofenac Potassium |
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| Non-Proprietary Name | Diclofenac Potassium |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 19981120 |
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| End Marketing Date | 20200831 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075229 |
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| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
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| Substance Name | DICLOFENAC POTASSIUM |
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| Strength | 50 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC] |
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