| NDC Code | 68071-4158-2 |
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| Package Description | 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4158-2) |
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| Product NDC | 68071-4158 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Diclofenac Sodium |
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| Non-Proprietary Name | Diclofenac Sodium |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20000228 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075492 |
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| Manufacturer | NuCare Pharmaceuticals,Inc. |
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| Substance Name | DICLOFENAC SODIUM |
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| Strength | 100 |
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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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