| NDC Code | 21922-009-09 |
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| Package Description | 1 TUBE in 1 CARTON (21922-009-09) > 100 g in 1 TUBE |
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| Product NDC | 21922-009 |
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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 Topical Gel, 1%, |
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| Dosage Form | GEL |
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| Usage | TOPICAL |
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| Start Marketing Date | 20200130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA210986 |
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| Manufacturer | Encube Ethicals Private Limited |
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| Substance Name | DICLOFENAC SODIUM |
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| Strength | 10 |
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| Strength Unit | mg/g |
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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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