Package 0781-1943-39

{"route": ["ORAL"], "spl_id": "047eb353-1ca4-419b-947c-4d418f87c22a", "openfda": {"upc": ["0307811943824"], "unii": ["804826J2HU", "544Y3D6MYH", "Q42OMW3AT8"], "rxcui": ["617995"], "spl_set_id": ["e41387c8-2c74-4990-831f-64dc921ee138"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "40 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE (0781-1943-39)", "package_ndc": "0781-1943-39", "marketing_start_date": "20100421"}, {"sample": false, "description": "28 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE (0781-1943-82)", "package_ndc": "0781-1943-82", "marketing_start_date": "20100421"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "0781-1943_047eb353-1ca4-419b-947c-4d418f87c22a", "dosage_form": "TABLET, MULTILAYER, EXTENDED RELEASE", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "0781-1943", "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": "562.5 mg/1"}, {"name": "AMOXICILLIN SODIUM", "strength": "437.5 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "62.5 mg/1"}], "application_number": "ANDA090227", "marketing_category": "ANDA", "marketing_start_date": "20100421", "listing_expiration_date": "20261231"}