Package 65862-535-02

{"route": ["ORAL"], "spl_id": "3d50990e-9d7e-4a23-a135-97d5612ec0bc", "openfda": {"upc": ["0365862535023"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617993"], "spl_set_id": ["5200ae31-8a79-45f9-84fc-98f8448483a7"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 mL in 1 BOTTLE (65862-535-02)", "package_ndc": "65862-535-02", "marketing_start_date": "20111220"}, {"sample": false, "description": "125 mL in 1 BOTTLE (65862-535-13)", "package_ndc": "65862-535-13", "marketing_start_date": "20111220"}, {"sample": false, "description": "75 mL in 1 BOTTLE (65862-535-75)", "package_ndc": "65862-535-75", "marketing_start_date": "20111220"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "65862-535_3d50990e-9d7e-4a23-a135-97d5612ec0bc", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "65862-535", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "600 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "42.9 mg/5mL"}], "application_number": "ANDA201091", "marketing_category": "ANDA", "marketing_start_date": "20111220", "listing_expiration_date": "20261231"}