| NDC Code | 51672-1358-4 |
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| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (51672-1358-4) / 60 mL in 1 BOTTLE, DROPPER |
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| Product NDC | 51672-1358 |
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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 | SOLUTION |
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| Usage | TOPICAL |
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| Start Marketing Date | 20141126 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203818 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | DICLOFENAC SODIUM |
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| Strength | 16.05 |
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| Strength Unit | mg/mL |
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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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