| NDC Code | 70069-501-01 |
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| Package Description | 1 BOTTLE in 1 CARTON (70069-501-01) / 10 mL in 1 BOTTLE |
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| Product NDC | 70069-501 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dorzolamide Hydrochloride |
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| Non-Proprietary Name | Dorzolamide Hydrochloride |
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| Dosage Form | SOLUTION/ DROPS |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 20250212 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215004 |
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| Manufacturer | Somerset Therapeutics, 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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