| NDC Code | 60290-057-03 |
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| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (60290-057-03) |
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| Product NDC | 60290-057 |
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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 Tablets |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20220512 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215750 |
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| Manufacturer | UMEDICA LABORATORIES PRIVATE LIMITED |
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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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