Package 0781-6139-54

{"route": ["ORAL"], "spl_id": "a64b73f7-9181-47db-9150-8ca6d2fbd189", "openfda": {"upc": ["0307816139574"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617993"], "spl_set_id": ["99b7f40a-06f9-4b97-8eee-8e61e5106aad"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 mL in 1 BOTTLE, DISPENSING (0781-6139-48)", "package_ndc": "0781-6139-48", "marketing_start_date": "20070813"}, {"sample": false, "description": "125 mL in 1 BOTTLE, DISPENSING (0781-6139-54)", "package_ndc": "0781-6139-54", "marketing_start_date": "20070813"}, {"sample": false, "description": "75 mL in 1 BOTTLE, DISPENSING (0781-6139-57)", "package_ndc": "0781-6139-57", "marketing_start_date": "20070813"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "0781-6139_a64b73f7-9181-47db-9150-8ca6d2fbd189", "dosage_form": "SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "0781-6139", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Sandoz Inc", "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": "ANDA065358", "marketing_category": "ANDA", "marketing_start_date": "20070813", "listing_expiration_date": "20261231"}