| NDC Code | 80539-001-39 |
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| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (80539-001-39) > 2.5 mL in 1 BOTTLE, PLASTIC |
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| Product NDC | 80539-001 |
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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 | 20200715 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA209995 |
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| Manufacturer | Allwell Health Inc |
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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 Inhibitor [EPC] |
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