Package 16714-294-01

{"route": ["ORAL"], "spl_id": "04e2b9cd-a5cb-4762-86f9-1afbd53b4bc6", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617993"], "spl_set_id": ["df4136c0-9efd-42c3-a487-e728e8b91275"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 mL in 1 BOTTLE (16714-294-01)", "package_ndc": "16714-294-01", "marketing_start_date": "20111220"}, {"sample": false, "description": "125 mL in 1 BOTTLE (16714-294-02)", "package_ndc": "16714-294-02", "marketing_start_date": "20111220"}, {"sample": false, "description": "200 mL in 1 BOTTLE (16714-294-03)", "package_ndc": "16714-294-03", "marketing_start_date": "20111220"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "16714-294_04e2b9cd-a5cb-4762-86f9-1afbd53b4bc6", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "16714-294", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amoxicillin and Clavulanate Potassium", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "600 mg/5mL"}, {"name": "CLAVULANATE POTASSIUM", "strength": "42.9 mg/5mL"}], "application_number": "ANDA201091", "marketing_category": "ANDA", "marketing_start_date": "20111220", "listing_expiration_date": "20261231"}