Package 16714-293-02

{"route": ["ORAL"], "spl_id": "581a5622-f3ca-4a4f-9241-9810694c791a", "openfda": {"unii": ["Q42OMW3AT8", "804826J2HU"], "rxcui": ["617423", "617430"], "spl_set_id": ["f0a6d21d-203f-4fde-b010-a2730b86b491"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (16714-293-01)", "package_ndc": "16714-293-01", "marketing_start_date": "20111220"}, {"sample": false, "description": "75 mL in 1 BOTTLE (16714-293-02)", "package_ndc": "16714-293-02", "marketing_start_date": "20111220"}, {"sample": false, "description": "100 mL in 1 BOTTLE (16714-293-03)", "package_ndc": "16714-293-03", "marketing_start_date": "20111220"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "16714-293_581a5622-f3ca-4a4f-9241-9810694c791a", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "16714-293", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "400 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "57 mg/5mL"}], "application_number": "ANDA201090", "marketing_category": "ANDA", "marketing_start_date": "20111220", "listing_expiration_date": "20261231"}