Package 70518-1536-2

{"route": ["ORAL"], "spl_id": "494ba843-28c3-dc71-e063-6394a90ac9cf", "openfda": {"nui": ["N0000175435", "M0014907"], "unii": ["140QMO216E"], "rxcui": ["314106"], "spl_set_id": ["cfeab9e3-58b9-4890-9185-11b62904e2af"], "pharm_class_cs": ["Nitroimidazoles [CS]"], "pharm_class_epc": ["Nitroimidazole Antimicrobial [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1536-2)", "package_ndc": "70518-1536-2", "marketing_start_date": "20240516"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1536-3)", "package_ndc": "70518-1536-3", "marketing_start_date": "20250530"}], "brand_name": "Metronidazole", "product_id": "70518-1536_494ba843-28c3-dc71-e063-6394a90ac9cf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Nitroimidazole Antimicrobial [EPC]", "Nitroimidazoles [CS]"], "product_ndc": "70518-1536", "generic_name": "Metronidazole", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metronidazole", "active_ingredients": [{"name": "METRONIDAZOLE", "strength": "250 mg/1"}], "application_number": "ANDA203458", "marketing_category": "ANDA", "marketing_start_date": "20181015", "listing_expiration_date": "20271231"}