Package 70518-4424-0

{"route": ["ORAL"], "spl_id": "4040e02b-8df8-0154-e063-6394a90a0980", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["562508"], "spl_set_id": ["704e99b1-c14a-40bf-adbd-c2794fa92c72"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4424-0)", "package_ndc": "70518-4424-0", "marketing_start_date": "20250805"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "70518-4424_4040e02b-8df8-0154-e063-6394a90a0980", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "70518-4424", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "REMEDYREPACK 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": "ANDA091568", "marketing_category": "ANDA", "marketing_start_date": "20250805", "listing_expiration_date": "20261231"}