Package 71335-2999-1

{"route": ["ORAL"], "spl_id": "6e01dd3f-c563-4091-a07f-52bbb6d51b0a", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617296"], "spl_set_id": ["22cd4e96-2288-470c-9264-8058cd7db9b0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-2999-1)", "package_ndc": "71335-2999-1", "marketing_start_date": "20251105"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "71335-2999_6e01dd3f-c563-4091-a07f-52bbb6d51b0a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "71335-2999", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Bryant Ranch Prepack", "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": "ANDA065064", "marketing_category": "ANDA", "marketing_start_date": "20020315", "listing_expiration_date": "20261231"}