| NDC Code | 50090-1615-1 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-1615-1) |
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| Product NDC | 50090-1615 |
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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 | 19960308 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA020254 |
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| Manufacturer | A-S Medication Solutions |
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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 | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
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