Package 73473-303-70

{"route": ["VAGINAL"], "spl_id": "a3efeca5-5c4b-432b-9537-ea2e1e67c17c", "openfda": {"nui": ["N0000175435", "M0014907"], "unii": ["140QMO216E"], "rxcui": ["142046"], "spl_set_id": ["94a83daa-6e34-419d-849a-6f18d3b8c586"], "pharm_class_cs": ["Nitroimidazoles [CS]"], "pharm_class_epc": ["Nitroimidazole Antimicrobial [EPC]"], "manufacturer_name": ["Solaris Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 CARTON (73473-303-70)  / 70 g in 1 TUBE, WITH APPLICATOR", "package_ndc": "73473-303-70", "marketing_start_date": "20260108"}], "brand_name": "Metronidazole", "product_id": "73473-303_a3efeca5-5c4b-432b-9537-ea2e1e67c17c", "dosage_form": "GEL", "pharm_class": ["Nitroimidazole Antimicrobial [EPC]", "Nitroimidazoles [CS]"], "product_ndc": "73473-303", "generic_name": "Metronidazole", "labeler_name": "Solaris Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metronidazole", "active_ingredients": [{"name": "METRONIDAZOLE", "strength": "7.5 mg/g"}], "application_number": "ANDA213648", "marketing_category": "ANDA", "marketing_start_date": "20260108", "listing_expiration_date": "20271231"}