| NDC Code | 70069-491-01 |
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| Package Description | 2.5 mL in 1 BOTTLE, PLASTIC (70069-491-01) |
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| Product NDC | 70069-491 |
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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/ DROPS |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 20241220 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215006 |
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| Manufacturer | Somerset Therapeutics, LLC |
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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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