| NDC Code | 61442-101-10 |
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| Package Description | 12 BOTTLE, PLASTIC in 1 BOX (61442-101-10) / 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC |
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| Product NDC | 61442-101 |
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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 | 19981113 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075185 |
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| Manufacturer | Carlsbad Technology, Inc. |
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| Substance Name | DICLOFENAC SODIUM |
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| Strength | 25 |
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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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