| NDC Code | 61314-320-01 |
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| Package Description | 1 BOTTLE in 1 CARTON (61314-320-01) > 30500 uL in 1 BOTTLE |
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| Product NDC | 61314-320 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Olopatadine Hydrochloride |
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| Non-Proprietary Name | Olopatadine Hydrochloride |
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| Dosage Form | SPRAY, METERED |
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| Usage | NASAL |
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| Start Marketing Date | 20150401 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA021861 |
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| Manufacturer | Sandoz Inc |
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| Substance Name | OLOPATADINE HYDROCHLORIDE |
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| Strength | 665 |
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| Strength Unit | ug/100uL |
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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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