| NDC Code | 73581-709-02 |
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| Package Description | 2 BOTTLE in 1 CARTON (73581-709-02) / 2.5 mL in 1 BOTTLE |
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| Product NDC | 73581-709 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Olopatadine Hydrochloride |
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| Non-Proprietary Name | Olopatadine Hydrochloride |
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| Dosage Form | SOLUTION |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 20260101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA219557 |
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| Manufacturer | YYBA Corp |
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| Substance Name | OLOPATADINE HYDROCHLORIDE |
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| Strength | 2 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Decreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Histamine-1 Receptor Inhibitor [EPC], Mast Cell Stabilizer [EPC] |
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