Package 68071-1619-1

{"route": ["ORAL"], "spl_id": "1d4c3bbf-43f9-8590-e063-6294a90adebb", "openfda": {"nui": ["N0000175930", "N0000000202"], "upc": ["0368071161915"], "unii": ["804826J2HU", "23521W1S24"], "rxcui": ["617430"], "spl_set_id": ["5d074fe6-1ee0-40d8-e053-2a91aa0a7549"], "pharm_class_epc": ["beta Lactamase Inhibitor [EPC]"], "pharm_class_moa": ["beta Lactamase Inhibitors [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68071-1619-1)", "package_ndc": "68071-1619-1", "marketing_start_date": "20171102"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "68071-1619_1d4c3bbf-43f9-8590-e063-6294a90adebb", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "68071-1619", "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": "400 mg/5mL"}, {"name": "CLAVULANIC ACID", "strength": "57 mg/5mL"}], "application_number": "ANDA065191", "marketing_category": "ANDA", "marketing_start_date": "20071201", "listing_expiration_date": "20261231"}