| NDC Code | 69367-209-01 |
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| Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69367-209-01) |
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| Product NDC | 69367-209 |
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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 | 20230420 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090779 |
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| Manufacturer | Westminster 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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