Package 65862-503-20

{"route": ["ORAL"], "spl_id": "2b91e9f8-c77e-4330-8fc1-e574758f0db6", "openfda": {"unii": ["Q42OMW3AT8", "804826J2HU"], "rxcui": ["562251", "562508", "617296"], "spl_set_id": ["ffb158a1-83ba-4100-9221-175aa986dc3e"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-503-01)", "package_ndc": "65862-503-01", "marketing_start_date": "20120120"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (65862-503-20)", "package_ndc": "65862-503-20", "marketing_start_date": "20120120"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "65862-503_2b91e9f8-c77e-4330-8fc1-e574758f0db6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "65862-503", "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": "875 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA091568", "marketing_category": "ANDA", "marketing_start_date": "20120120", "listing_expiration_date": "20261231"}