| NDC Code | 71921-400-10 |
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| Package Description | 10 mL in 1 BOTTLE (71921-400-10) |
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| Product NDC | 71921-400 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dorzolamide Hydrochloride Ophthalmic |
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| Non-Proprietary Name | Dorzolamide Hydrochloride Ophthalmic |
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| Dosage Form | SOLUTION |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 20250507 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202053 |
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| Manufacturer | Florida Pharmaceutical Products, LLC |
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| Substance Name | DORZOLAMIDE HYDROCHLORIDE |
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| Strength | 20 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Carbonic Anhydrase Inhibitor [EPC], Carbonic Anhydrase Inhibitors [MoA] |
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