Package 68071-3842-2

{"route": ["ORAL"], "spl_id": "348f7f87-48ae-4cb4-e063-6394a90aa5fe", "openfda": {"upc": ["0368071384222"], "unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["348f7f77-ba7e-5dd9-e063-6294a90a0991"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-3842-2)", "package_ndc": "68071-3842-2", "marketing_start_date": "20250507"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68071-3842_348f7f87-48ae-4cb4-e063-6394a90aa5fe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68071-3842", "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": "875 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "ANDA065063", "marketing_category": "ANDA", "marketing_start_date": "20220801", "listing_expiration_date": "20261231"}