| NDC Code | 0093-7618-43 |
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| Package Description | 1 BOTTLE in 1 CARTON (0093-7618-43) > 10 mL in 1 BOTTLE |
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| Product NDC | 0093-7618 |
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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 |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 20100128 |
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| End Marketing Date | 20190531 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078756 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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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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