| NDC Code | 50742-233-01 |
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| Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50742-233-01) |
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| Product NDC | 50742-233 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Acetazolamide |
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| Non-Proprietary Name | Acetazolamide |
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| Dosage Form | CAPSULE, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20170731 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203434 |
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| Manufacturer | Ingenus Pharmaceuticals, LLC |
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| Substance Name | ACETAZOLAMIDE |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Carbonic Anhydrase Inhibitor [EPC], Carbonic Anhydrase Inhibitors [MoA], Sulfonamides [CS] |
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