Package 68682-455-70

{"route": ["VAGINAL"], "spl_id": "65a9e9bc-c5ac-401a-addf-2d83b0df83a8", "openfda": {"nui": ["N0000175435", "M0014907"], "unii": ["140QMO216E"], "rxcui": ["142046"], "spl_set_id": ["526c226a-099b-4eb3-943d-c88b2763b2c1"], "pharm_class_cs": ["Nitroimidazoles [CS]"], "pharm_class_epc": ["Nitroimidazole Antimicrobial [EPC]"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 CARTON (68682-455-70)  / 70 g in 1 TUBE, WITH APPLICATOR", "package_ndc": "68682-455-70", "marketing_start_date": "20150401"}], "brand_name": "Metronidazole", "product_id": "68682-455_65a9e9bc-c5ac-401a-addf-2d83b0df83a8", "dosage_form": "GEL", "pharm_class": ["Nitroimidazole Antimicrobial [EPC]", "Nitroimidazoles [CS]"], "product_ndc": "68682-455", "generic_name": "metronidazole", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metronidazole", "active_ingredients": [{"name": "METRONIDAZOLE", "strength": "7.5 mg/g"}], "application_number": "NDA020208", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20150401", "listing_expiration_date": "20261231"}