Package 68071-4275-2

{"route": ["ORAL"], "spl_id": "1a3dc0d3-89e5-ab47-e063-6394a90a1952", "openfda": {"upc": ["0368071427523"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617296"], "spl_set_id": ["64a27ad7-4d32-69c8-e053-2a91aa0aa967"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-4275-2)", "package_ndc": "68071-4275-2", "marketing_start_date": "20180207"}], "brand_name": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "product_id": "68071-4275_1a3dc0d3-89e5-ab47-e063-6394a90a1952", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68071-4275", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "500 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA205707", "marketing_category": "ANDA", "marketing_start_date": "20170301", "listing_expiration_date": "20261231"}