Package 0093-8675-75

{"route": ["ORAL"], "spl_id": "2faf9b29-5df4-4f3c-84d9-6866f91b87e8", "openfda": {"unii": ["804826J2HU", "Q42OMW3AT8"], "rxcui": ["617993"], "spl_set_id": ["e83f43dd-f79e-4166-9bee-9427e235c876"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 mL in 1 BOTTLE (0093-8675-74)", "package_ndc": "0093-8675-74", "marketing_start_date": "20040923"}, {"sample": false, "description": "125 mL in 1 BOTTLE (0093-8675-75)", "package_ndc": "0093-8675-75", "marketing_start_date": "20040923"}, {"sample": false, "description": "75 mL in 1 BOTTLE (0093-8675-78)", "package_ndc": "0093-8675-78", "marketing_start_date": "20040923"}], "brand_name": "Amoxicillin and Clavulanate Potassium", "product_id": "0093-8675_2faf9b29-5df4-4f3c-84d9-6866f91b87e8", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "0093-8675", "generic_name": "Amoxicillin and Clavulanate Potassium", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "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": "ANDA065162", "marketing_category": "ANDA", "marketing_start_date": "20040923", "listing_expiration_date": "20271231"}