| NDC Code | 71337-046-05 |
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| Package Description | 500 TABLET in 1 BOTTLE (71337-046-05) |
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| Product NDC | 71337-046 |
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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, Film Coated |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20230625 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215787 |
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| Manufacturer | Havix Group Inc d-b-a Aavis Pharmaceuticals |
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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 | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC] |
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