Package 61919-032-10

{"route": ["ORAL"], "spl_id": "47e13e06-0078-1557-e063-6294a90a5f79", "openfda": {"nui": ["N0000175435", "M0014907"], "unii": ["140QMO216E"], "rxcui": ["311681"], "spl_set_id": ["90a5acb3-f8cc-1e82-e053-2995a90a4e97"], "pharm_class_cs": ["Nitroimidazoles [CS]"], "pharm_class_epc": ["Nitroimidazole Antimicrobial [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (61919-032-10)", "package_ndc": "61919-032-10", "marketing_start_date": "20190821"}], "brand_name": "METRONIDAZOLE", "product_id": "61919-032_47e13e06-0078-1557-e063-6294a90a5f79", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Nitroimidazole Antimicrobial [EPC]", "Nitroimidazoles [CS]"], "product_ndc": "61919-032", "generic_name": "METRONIDAZOLE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METRONIDAZOLE", "active_ingredients": [{"name": "METRONIDAZOLE", "strength": "500 mg/1"}], "application_number": "ANDA203458", "marketing_category": "ANDA", "marketing_start_date": "20190821", "listing_expiration_date": "20271231"}