| NDC Code | 70934-122-90 |
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| Package Description | 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70934-122-90) |
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| Product NDC | 70934-122 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Diclofenac Sodium |
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| Proprietary Name Suffix | Delayed Release |
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| Non-Proprietary Name | Diclofenac Sodium |
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| Dosage Form | TABLET, DELAYED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20181108 |
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| End Marketing Date | 20250731 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075185 |
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| Manufacturer | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
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| Substance Name | DICLOFENAC SODIUM |
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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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