Package 70505-100-10

{"route": ["ORAL"], "spl_id": "59e091eb-f626-4083-b134-8d648d28b918", "openfda": {"unii": ["V9BI9B5YI2", "68Y4CF58BV"], "rxcui": ["1375948"], "spl_set_id": ["76d10d65-0279-4e86-8104-cade4343f839"], "manufacturer_name": ["Analog Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (70505-100-10)", "package_ndc": "70505-100-10", "marketing_start_date": "20181115"}], "brand_name": "Doxylamine succinate and pyridoxine hydrochloride", "product_id": "70505-100_59e091eb-f626-4083-b134-8d648d28b918", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Analogs/Derivatives [Chemical/Ingredient]", "Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]", "Vitamin B 6 [Chemical/Ingredient]", "Vitamin B6 Analog [EPC]"], "product_ndc": "70505-100", "generic_name": "Doxylamine succinate and pyridoxine hydrochloride", "labeler_name": "Analog Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxylamine succinate and pyridoxine hydrochloride", "active_ingredients": [{"name": "DOXYLAMINE SUCCINATE", "strength": "10 mg/1"}, {"name": "PYRIDOXINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA021876", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20181115", "listing_expiration_date": "20261231"}