| NDC Code | 72657-121-50 |
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| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (72657-121-50) / 5 mL in 1 BOTTLE, PLASTIC |
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| Product NDC | 72657-121 |
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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 Ophthalmic |
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| Dosage Form | SOLUTION |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 20240726 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA200810 |
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| Manufacturer | GLENMARK THERAPEUTICS INC., USA |
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| Substance Name | OLOPATADINE HYDROCHLORIDE |
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| Strength | 1 |
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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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